Canonical Allele Identifier: CA1374121573
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266815C= , CM000665.2:g.72266815C= GRCh38
NC_000003.11:g.72315966C= , CM000665.1:g.72315966C= GRCh37
NC_000003.10:g.72398656C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8293G=