Canonical Allele Identifier: CA1619157084
Gene:

Linked Data

dbSNP Id: rs1241225767

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439816C>A , CM000668.2:g.31439816C>A GRCh38
NC_000006.11:g.31407593C>A , CM000668.1:g.31407593C>A GRCh37
NC_000006.10:g.31515572C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.291G>T