LDH info

Canonical Allele Identifier: CA10590055
Gene: GRIN2D HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 267211
ClinVar RCV Id: RCV000257970
dbSNP Id: rs886040861

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419722G>A , CM000681.2:g.48419722G>A GRCh38
NC_000019.9:g.48922979G>A , CM000681.1:g.48922979G>A GRCh37
NC_000019.8:g.53614791G>A NCBI36
NG_052829.1:g.29848G>A

Transcript Alleles

HGVS Amino-acid change
NM_000836.2:c.1999G>A VV NP_000827.2:p.Val667Ile
XM_011526872.1:c.1999G>A XP_011525174.1:p.Val667Ile
ENST00000263269.3:c.1999G>A ENSP00000263269.2:p.Val667Ile