Canonical Allele Identifier: CA15790807
Gene: DGKH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1012053

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42079301C>A , CM000675.2:g.42079301C>A GRCh38
NC_000013.10:g.42653437C>A , CM000675.1:g.42653437C>A GRCh37
NC_000013.9:g.41551437C>A NCBI36
NG_029191.2:g.44266C>A
NG_029191.3:g.44266C>A

Transcript Alleles

HGVS Amino-acid change
NM_001204504.2:c.192+30336C>A VV NP_001191433.1:p.=
NM_152910.5:c.192+30336C>A VV NP_690874.2:p.=
NM_178009.4:c.192+30336C>A VV NP_821077.1:p.=
ENST00000261491.9:c.192+30336C>A ENSP00000261491.4:p.=
ENST00000337343.8:c.192+30336C>A ENSP00000337572.4:p.=
ENST00000379274.6:c.192+30336C>A ENSP00000368576.3:p.=