Canonical Allele Identifier: CA1691656443
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957849C= , CM000669.2:g.17957849C= GRCh38
NC_000007.13:g.17997472C= , CM000669.1:g.17997472C= GRCh37
NC_000007.12:g.17963997C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-821C=