Canonical Allele Identifier: CA1481407444
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501263G= , CM000666.2:g.102501263G= GRCh38
NC_000004.11:g.103422420G= , CM000666.1:g.103422420G= GRCh37
NC_000004.10:g.103641452G= NCBI36
NG_050628.1:g.4935G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.629C= XP_011530769.1:p.Ala210=
NR_136202.1:n.48+1176C=