Canonical Allele Identifier: CA2774472376
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400575C>G , CM000669.2:g.13400575C>G GRCh38
NC_000007.13:g.13440200C>G , CM000669.1:g.13440200C>G GRCh37
NC_000007.12:g.13406725C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90252C>G