Canonical Allele Identifier: CA1284674135
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883975C= , CM000664.2:g.122883975C= GRCh38
NC_000002.11:g.123641551C= , CM000664.1:g.123641551C= GRCh37
NC_000002.10:g.123358021C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-967C=
XR_001739692.1:n.1451-967C=
XR_923292.2:n.1358-967C=