Canonical Allele Identifier: CA1320446089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033071G= , CM000664.2:g.200033071G= GRCh38
NC_000002.11:g.200897794G= , CM000664.1:g.200897794G= GRCh37
NC_000002.10:g.200606039G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22175C=