LDH info

Canonical Allele Identifier: CA119766
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 8585
ClinVar RCV Id: RCV000009116
dbSNP Id: rs28936387

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56879153T>C , CM000678.2:g.56879153T>C GRCh38
NC_000016.9:g.56913065T>C , CM000678.1:g.56913065T>C GRCh37
NC_000016.8:g.55470566T>C NCBI36
NG_009386.1:g.18947T>C

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.1261T>C VV NP_000330.2:p.Cys421Arg
NM_001126107.1:c.1258T>C VV NP_001119579.1:p.Cys420Arg
NM_001126108.1:c.1261T>C VV NP_001119580.1:p.Cys421Arg
XM_005256119.1:c.1258T>C XP_005256176.1:p.Cys420Arg
XM_005256119.2:c.1258T>C XP_005256176.1:p.Cys420Arg
ENST00000262502.5:c.1258T>C ENSP00000262502.5:p.Cys420Arg
ENST00000438926.6:c.1261T>C ENSP00000402152.2:p.Cys421Arg
ENST00000563236.5:c.1261T>C ENSP00000456149.1:p.Cys421Arg
ENST00000566786.5:c.1258T>C ENSP00000457552.1:p.Cys420Arg