Canonical Allele Identifier: CA1691656512
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957974C= , CM000669.2:g.17957974C= GRCh38
NC_000007.13:g.17997597C= , CM000669.1:g.17997597C= GRCh37
NC_000007.12:g.17964122C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-696C=