LDH info

Canonical Allele Identifier: CA255471
Gene: NDP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10684
ClinVar RCV Id: RCV000011430
dbSNP Id: rs28933684

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949831G>A , CM000685.2:g.43949831G>A GRCh38
NC_000023.10:g.43809077G>A , CM000685.1:g.43809077G>A GRCh37
NC_000023.9:g.43694021G>A NCBI36
NG_009832.1:g.28845C>T

Transcript Alleles

HGVS Amino-acid change
NM_000266.3:c.370C>T VV NP_000257.1:p.Leu124Phe
NR_046631.1:n.100G>A
NM_000266.4:c.370C>T VV MANE Preferred NP_000257.1:p.Leu124Phe
ENST00000378062.5:c.370C>T ENSP00000367301.5:p.Leu124Phe
ENST00000470584.1:n.414C>T