Canonical Allele Identifier: CA1740470190
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306503C= , CM000669.2:g.124306503C= GRCh38
NC_000007.13:g.123946557C= , CM000669.1:g.123946557C= GRCh37
NC_000007.12:g.123733793C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.98C=