Canonical Allele Identifier: CA1267947385
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016202C= , CM000664.2:g.88016202C= GRCh38
NC_000002.11:g.88315721C= , CM000664.1:g.88315721C= GRCh37
NC_000002.10:g.88096836C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.547C=
XR_940336.3:n.547C=