LDH info

Canonical Allele Identifier: CA118837
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 7486
dbSNP Id: rs11200638

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461028G>A , CM000672.2:g.122461028G>A GRCh38
NC_000010.10:g.124220544G>A , CM000672.1:g.124220544G>A GRCh37
NC_000010.9:g.124210534G>A NCBI36
NG_011554.1:g.4504G>A

Transcript Alleles

HGVS Amino-acid change
XR_946382.1:n.331C>T
XR_946383.1:n.331C>T
XR_946384.1:n.331C>T
XR_946385.1:n.331C>T
XR_946382.2:n.359C>T
XR_946383.2:n.359C>T
XR_946384.2:n.335C>T
XR_946385.2:n.359C>T