Canonical Allele Identifier: CA1481407419
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501252C= , CM000666.2:g.102501252C= GRCh38
NC_000004.11:g.103422409C= , CM000666.1:g.103422409C= GRCh37
NC_000004.10:g.103641441C= NCBI36
NG_050628.1:g.4924C=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.640G= XP_011530769.1:p.Gly214=
NR_136202.1:n.48+1187G=