Canonical Allele Identifier: CA1284674155
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884004A= , CM000664.2:g.122884004A= GRCh38
NC_000002.11:g.123641580A= , CM000664.1:g.123641580A= GRCh37
NC_000002.10:g.123358050A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-938A=
XR_001739692.1:n.1451-938A=
XR_923292.2:n.1358-938A=