LDH info

Canonical Allele Identifier: CA119778
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 8594
ClinVar RCV Id: RCV000009125
dbSNP Id: rs121909384

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56885328G>T , CM000678.2:g.56885328G>T GRCh38
NC_000016.9:g.56919240G>T , CM000678.1:g.56919240G>T GRCh37
NC_000016.8:g.55476741G>T NCBI36
NG_009386.1:g.25122G>T

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.1889G>T VV NP_000330.2:p.Gly630Val
NM_001126107.1:c.1886G>T VV NP_001119579.1:p.Gly629Val
NM_001126108.1:c.1889G>T VV NP_001119580.1:p.Gly630Val
XM_005256119.1:c.1886G>T XP_005256176.1:p.Gly629Val
XM_005256119.2:c.1886G>T XP_005256176.1:p.Gly629Val
ENST00000262502.5:c.1886G>T ENSP00000262502.5:p.Gly629Val
ENST00000438926.6:c.1889G>T ENSP00000402152.2:p.Gly630Val
ENST00000563236.5:c.1889G>T ENSP00000456149.1:p.Gly630Val
ENST00000566786.5:c.1886G>T ENSP00000457552.1:p.Gly629Val