LDH info

Canonical Allele Identifier: CA142803
Gene: OTOF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21836
dbSNP Id: rs13031859

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26519093G>A , CM000664.2:g.26519093G>A GRCh38
NC_000002.11:g.26741961G>A , CM000664.1:g.26741961G>A GRCh37
NC_000002.10:g.26595465G>A NCBI36
NG_009937.1:g.44606C>T

Transcript Alleles

HGVS Amino-acid change
NM_001287489.1:c.244C>T VV NP_001274418.1:p.Arg82Cys
NM_194248.2:c.244C>T VV NP_919224.1:p.Arg82Cys
XM_005264644.2:n.244C>T XP_005264701.1:p.Arg82Cys
XM_011533185.1:n.244C>T XP_011531487.1:p.Arg82Cys
XM_017005338.1:n.244C>T XP_016860827.1:p.Arg82Cys
NM_001287489.2:c.244C>T VV NP_001274418.1:p.Arg82Cys
NM_194248.3:c.244C>T VV MANE Preferred NP_919224.1:p.Arg82Cys
ENST00000272371.6:c.244C>T ENSP00000272371.2:p.Arg82Cys
ENST00000403946.7:c.244C>T ENSP00000385255.3:p.Arg82Cys