Canonical Allele Identifier: CA13786933
Gene: DGKH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1170191

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42101357A>G , CM000675.2:g.42101357A>G GRCh38
NC_000013.10:g.42675493A>G , CM000675.1:g.42675493A>G GRCh37
NC_000013.9:g.41573493A>G NCBI36
NG_029191.2:g.66322A>G
NG_029191.3:g.66322A>G

Transcript Alleles

HGVS Amino-acid change
NM_001204504.2:c.193-26106A>G VV NP_001191433.1:p.=
NM_152910.5:c.193-26106A>G VV NP_690874.2:p.=
NM_178009.4:c.193-26106A>G VV NP_821077.1:p.=
ENST00000261491.9:c.193-26106A>G ENSP00000261491.4:p.=
ENST00000337343.8:c.193-26106A>G ENSP00000337572.4:p.=
ENST00000379274.6:c.193-26106A>G ENSP00000368576.3:p.=