Canonical Allele Identifier: CA1481407435
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501258C= , CM000666.2:g.102501258C= GRCh38
NC_000004.11:g.103422415C= , CM000666.1:g.103422415C= GRCh37
NC_000004.10:g.103641447C= NCBI36
NG_050628.1:g.4930C=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.634G= XP_011530769.1:p.Gly212=
NR_136202.1:n.48+1181G=