Canonical Allele Identifier: CA1267947369
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016189C= , CM000664.2:g.88016189C= GRCh38
NC_000002.11:g.88315708C= , CM000664.1:g.88315708C= GRCh37
NC_000002.10:g.88096823C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.534C=
XR_940336.3:n.534C=