LDH info

Canonical Allele Identifier: CA119768
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 8586
ClinVar RCV Id: RCV000009117
dbSNP Id: rs28936388

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56870119C>T , CM000678.2:g.56870119C>T GRCh38
NC_000016.9:g.56904031C>T , CM000678.1:g.56904031C>T GRCh37
NC_000016.8:g.55461532C>T NCBI36
NG_009386.1:g.9913C>T

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.625C>T VV NP_000330.2:p.Arg209Trp
NM_001126107.1:c.622C>T VV NP_001119579.1:p.Arg208Trp
NM_001126108.1:c.625C>T VV NP_001119580.1:p.Arg209Trp
XM_005256119.1:c.622C>T XP_005256176.1:p.Arg208Trp
XM_005256119.2:c.622C>T XP_005256176.1:p.Arg208Trp
ENST00000262502.5:c.622C>T ENSP00000262502.5:p.Arg208Trp
ENST00000438926.6:c.625C>T ENSP00000402152.2:p.Arg209Trp
ENST00000563236.5:c.625C>T ENSP00000456149.1:p.Arg209Trp
ENST00000566786.5:c.622C>T ENSP00000457552.1:p.Arg208Trp