Canonical Allele Identifier: CA1704461084
Community Standard Title: NC_000007.14:g.45942861T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45942861T= , CM000669.2:g.45942861T= GRCh38
NC_000007.13:g.45982460T= , CM000669.1:g.45982460T= GRCh37
NC_000007.12:g.45948985T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745202.1:n.326+1981T=
XR_001745203.1:n.326+1981T=
XR_927237.1:n.321+1981T=
XR_927238.1:n.321+1981T=
XR_927239.1:n.321+1981T=
XR_927240.1:n.321+1981T=