Canonical Allele Identifier: CA1740470132
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306374T= , CM000669.2:g.124306374T= GRCh38
NC_000007.13:g.123946428T= , CM000669.1:g.123946428T= GRCh37
NC_000007.12:g.123733664T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-104T=