Canonical Allele Identifier: CA125569078
Gene:

Linked Data

dbSNP Id: rs766863769

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660928C>G , CM000667.2:g.113660928C>G GRCh38
NC_000005.9:g.112996625C>G , CM000667.1:g.112996625C>G GRCh37
NC_000005.8:g.113024524C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27564C>G