Canonical Allele Identifier: CA1267947189
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015966A= , CM000664.2:g.88015966A= GRCh38
NC_000002.11:g.88315485A= , CM000664.1:g.88315485A= GRCh37
NC_000002.10:g.88096600A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.311A=
XR_940336.3:n.311A=