Canonical Allele Identifier: CA1267947442
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016244C= , CM000664.2:g.88016244C= GRCh38
NC_000002.11:g.88315763C= , CM000664.1:g.88315763C= GRCh37
NC_000002.10:g.88096878C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.589C=
XR_940336.3:n.589C=