Canonical Allele Identifier: CA1691656437
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957839C= , CM000669.2:g.17957839C= GRCh38
NC_000007.13:g.17997462C= , CM000669.1:g.17997462C= GRCh37
NC_000007.12:g.17963987C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-831C=