Canonical Allele Identifier: CA1211363870
Gene:

Linked Data

dbSNP Id: rs10911021

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182112825C>A , CM000663.2:g.182112825C>A GRCh38
NC_000001.10:g.182081960C>A , CM000663.1:g.182081960C>A GRCh37
NC_000001.9:g.180348583C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922341.1:n.243-2426C>A
XR_922341.2:n.334-2426C>A