LDH info

Canonical Allele Identifier: CA250046
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 8584
ClinVar RCV Id: RCV000009115
dbSNP Id: rs121909379

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56894558T>C , CM000678.2:g.56894558T>C GRCh38
NC_000016.9:g.56928470T>C , CM000678.1:g.56928470T>C GRCh37
NC_000016.8:g.55485971T>C NCBI36
NG_009386.1:g.34352T>C

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.2576T>C VV NP_000330.2:p.Leu859Pro
NM_001126107.1:c.2573T>C VV NP_001119579.1:p.Leu858Pro
NM_001126108.1:c.2549T>C VV NP_001119580.1:p.Leu850Pro
XM_005256119.1:c.2546T>C XP_005256176.1:p.Leu849Pro
XM_005256119.2:c.2546T>C XP_005256176.1:p.Leu849Pro
ENST00000262502.5:c.2546T>C ENSP00000262502.5:p.Leu849Pro
ENST00000438926.6:c.2576T>C ENSP00000402152.2:p.Leu859Pro
ENST00000563236.5:c.2549T>C ENSP00000456149.1:p.Leu850Pro
ENST00000566786.5:c.2573T>C ENSP00000457552.1:p.Leu858Pro