LDH info

Canonical Allele Identifier: CA255481
Gene: NDP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10694
ClinVar RCV Id: RCV000011440
dbSNP Id: rs104894876

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949873A>C , CM000685.2:g.43949873A>C GRCh38
NC_000023.10:g.43809119A>C , CM000685.1:g.43809119A>C GRCh37
NC_000023.9:g.43694063A>C NCBI36
NG_009832.1:g.28803T>G

Transcript Alleles

HGVS Amino-acid change
NM_000266.3:c.328T>G VV NP_000257.1:p.Cys110Gly
NR_046631.1:n.142A>C
NM_000266.4:c.328T>G VV MANE Preferred NP_000257.1:p.Cys110Gly
ENST00000378062.5:c.328T>G ENSP00000367301.5:p.Cys110Gly
ENST00000470584.1:n.372T>G