Canonical Allele Identifier: CA1481406986
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500977T= , CM000666.2:g.102500977T= GRCh38
NC_000004.11:g.103422134T= , CM000666.1:g.103422134T= GRCh37
NC_000004.10:g.103641166T= NCBI36
NG_050628.1:g.4649T=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+272A= XP_011530769.1:n.643+272A=
NR_136202.1:n.48+1462A=