LDH info

Canonical Allele Identifier: CA118439
Gene: NOG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6707
ClinVar RCV Id: RCV000007099
dbSNP Id: rs104894615

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594838G>C , CM000679.2:g.56594838G>C GRCh38
NC_000017.10:g.54672199G>C , CM000679.1:g.54672199G>C GRCh37
NC_000017.9:g.52027198G>C NCBI36
NG_011958.1:g.6140G>C

Transcript Alleles

HGVS Amino-acid change
NM_005450.4:c.615G>C VV NP_005441.1:p.Trp205Cys
NM_005450.6:c.615G>C VV NP_005441.1:p.Trp205Cys
ENST00000332822.4:c.615G>C ENSP00000328181.4:p.Trp205Cys