Canonical Allele Identifier: CA1267947432
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016237C= , CM000664.2:g.88016237C= GRCh38
NC_000002.11:g.88315756C= , CM000664.1:g.88315756C= GRCh37
NC_000002.10:g.88096871C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.582C=
XR_940336.3:n.582C=