Canonical Allele Identifier: CA125569076
Gene:

Linked Data

dbSNP Id: rs952813278

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660916G>A , CM000667.2:g.113660916G>A GRCh38
NC_000005.9:g.112996613G>A , CM000667.1:g.112996613G>A GRCh37
NC_000005.8:g.113024512G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27552G>A