Canonical Allele Identifier: CA1284674112
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883950C= , CM000664.2:g.122883950C= GRCh38
NC_000002.11:g.123641526C= , CM000664.1:g.123641526C= GRCh37
NC_000002.10:g.123357996C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-992C=
XR_001739692.1:n.1451-992C=
XR_923292.2:n.1358-992C=