Canonical Allele Identifier: CA2833389268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016120C>A , CM000664.2:g.88016120C>A GRCh38
NC_000002.11:g.88315639C>A , CM000664.1:g.88315639C>A GRCh37
NC_000002.10:g.88096754C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.465C>A
XR_940336.3:n.465C>A