Canonical Allele Identifier: CA1374121568
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266808C= , CM000665.2:g.72266808C= GRCh38
NC_000003.11:g.72315959C= , CM000665.1:g.72315959C= GRCh37
NC_000003.10:g.72398649C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8300G=