LDH info

Canonical Allele Identifier: CA345098
Gene: OTOF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 65784
ClinVar RCV Id: RCV000056023
dbSNP Id: rs397515589

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480274C>T , CM000664.2:g.26480274C>T GRCh38
NC_000002.11:g.26703142C>T , CM000664.1:g.26703142C>T GRCh37
NC_000002.10:g.26556646C>T NCBI36
NG_009937.1:g.83425G>A

Transcript Alleles

HGVS Amino-acid change
NM_001287489.1:c.1841G>A VV NP_001274418.1:p.Gly614Glu
NM_194248.2:c.1841G>A VV NP_919224.1:p.Gly614Glu
XM_005264644.2:n.1886G>A XP_005264701.1:p.Gly629Glu
XM_011533185.1:n.1886G>A XP_011531487.1:p.Gly629Glu
XM_017005338.1:n.1841G>A XP_016860827.1:p.Gly614Glu
NM_001287489.2:c.1841G>A VV NP_001274418.1:p.Gly614Glu
NM_194248.3:c.1841G>A VV MANE Preferred NP_919224.1:p.Gly614Glu
ENST00000272371.6:c.1841G>A ENSP00000272371.2:p.Gly614Glu
ENST00000403946.7:c.1841G>A ENSP00000385255.3:p.Gly614Glu