Canonical Allele Identifier: CA1284674049
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883867A= , CM000664.2:g.122883867A= GRCh38
NC_000002.11:g.123641443A= , CM000664.1:g.123641443A= GRCh37
NC_000002.10:g.123357913A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1075A=
XR_001739692.1:n.1451-1075A=
XR_923292.2:n.1358-1075A=