LDH info

Canonical Allele Identifier: CA255948
Gene: SLC16A2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11640
ClinVar RCV Id: RCV000012406
dbSNP Id: rs104894940

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525844C>A , CM000685.2:g.74525844C>A GRCh38
NC_000023.10:g.73745679C>A , CM000685.1:g.73745679C>A GRCh37
NC_000023.9:g.73662404C>A NCBI36
NG_011641.1:g.109595C>A
NG_011641.2:g.109595C>A

Transcript Alleles

HGVS Amino-acid change
NM_006517.4:c.1121C>A VV NP_006508.2:p.Ser374Ter
XM_005262294.1:c.1121C>A XP_005262351.1:p.Ser374Ter
NM_006517.5:c.1121C>A VV MANE Preferred NP_006508.2:p.Ser374Ter
ENST00000587091.5:c.1121C>A ENSP00000465734.1:p.Ser374Ter
ENST00000590447.1:n.561C>A