Canonical Allele Identifier: CA1284674198
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884058A= , CM000664.2:g.122884058A= GRCh38
NC_000002.11:g.123641634A= , CM000664.1:g.123641634A= GRCh37
NC_000002.10:g.123358104A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-884A=
XR_001739692.1:n.1451-884A=
XR_923292.2:n.1358-884A=