Canonical Allele Identifier: CA1118991769
Gene:

Linked Data

dbSNP Id: rs1814931663

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999157G>A , CM000670.2:g.126999157G>A GRCh38
NC_000008.10:g.128011402G>A , CM000670.1:g.128011402G>A GRCh37
NC_000008.9:g.128080584G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7398G>A