Canonical Allele Identifier: CA802120415
Gene:

Linked Data

dbSNP Id: rs1244602365

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661005A>G , CM000667.2:g.113661005A>G GRCh38
NC_000005.9:g.112996702A>G , CM000667.1:g.112996702A>G GRCh37
NC_000005.8:g.113024601A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27641A>G