LDH info

Canonical Allele Identifier: CA8070053
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 319917
ClinVar RCV Id: RCV000405253
dbSNP Id: rs12708965

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56902407C>T , CM000678.2:g.56902407C>T GRCh38
NC_000016.9:g.56936319C>T , CM000678.1:g.56936319C>T GRCh37
NC_000016.8:g.55493820C>T NCBI36
NG_009386.1:g.42201C>T

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.2782C>T VV NP_000330.2:p.Arg928Cys
NM_001126107.1:c.2779C>T VV NP_001119579.1:p.Arg927Cys
NM_001126108.1:c.2755C>T VV NP_001119580.1:p.Arg919Cys
XM_005256119.1:c.2752C>T XP_005256176.1:p.Arg918Cys
XM_005256119.2:c.2752C>T XP_005256176.1:p.Arg918Cys
ENST00000262502.5:c.2752C>T ENSP00000262502.5:p.Arg918Cys
ENST00000438926.6:c.2782C>T ENSP00000402152.2:p.Arg928Cys
ENST00000563236.5:c.2755C>T ENSP00000456149.1:p.Arg919Cys
ENST00000566786.5:c.2779C>T ENSP00000457552.1:p.Arg927Cys
ENST00000569002.1:n.186C>T