Canonical Allele Identifier: CA1691656513
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957981C= , CM000669.2:g.17957981C= GRCh38
NC_000007.13:g.17997604C= , CM000669.1:g.17997604C= GRCh37
NC_000007.12:g.17964129C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-689C=