LDH info

Canonical Allele Identifier: CA118429
Gene: NOG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6695
ClinVar RCV Id: RCV000007083
dbSNP Id: rs104894609

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594788G>T , CM000679.2:g.56594788G>T GRCh38
NC_000017.10:g.54672149G>T , CM000679.1:g.54672149G>T GRCh37
NC_000017.9:g.52027148G>T NCBI36
NG_011958.1:g.6090G>T

Transcript Alleles

HGVS Amino-acid change
NM_005450.4:c.565G>T VV NP_005441.1:p.Gly189Cys
NM_005450.6:c.565G>T VV MANE Preferred NP_005441.1:p.Gly189Cys
ENST00000332822.4:c.565G>T ENSP00000328181.4:p.Gly189Cys