Canonical Allele Identifier: CA2774472377
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400641T>G , CM000669.2:g.13400641T>G GRCh38
NC_000007.13:g.13440266T>G , CM000669.1:g.13440266T>G GRCh37
NC_000007.12:g.13406791T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.147+90318T>G