Canonical Allele Identifier: CA1481406898
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500933A= , CM000666.2:g.102500933A= GRCh38
NC_000004.11:g.103422090A= , CM000666.1:g.103422090A= GRCh37
NC_000004.10:g.103641122A= NCBI36
NG_050628.1:g.4605A=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+316T= XP_011530769.1:n.643+316T=
NR_136202.1:n.48+1506T=