Canonical Allele Identifier: CA15137857
Gene:

Linked Data

dbSNP Id: rs10916248

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068646A>T , CM000663.2:g.224068646A>T GRCh38
NC_000001.10:g.224256348A>T , CM000663.1:g.224256348A>T GRCh37
NC_000001.9:g.222322971A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+992A>T
XR_001737824.1:n.242+992A>T