Sequence alignments between the human reference sequence, GRCh37, and the genomes of Venter and Watson. Variation data are highlighted in green and indicated by an IUPAC code. A. The default display replaces nucleotides with dots if the genome has the same allele as the reference assembly. B. The display can be changed by using the matching basepairs: show all option in the configure this page link. http://Mar2010.archive.ensembl.org/Homo_sapiens/Location/SequenceAlignment?db=core;g=ENSG00000134242;r=1:114382907-114387906;t=ENST00000359785 webcite.
Chen et al. BMC Genomics 2010 11:293 doi:10.1186/1471-2164-11-293