LDH info

Canonical Allele Identifier: CA145312
Gene: GRIN2A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 88728
ClinVar RCV Id: RCV000074387
dbSNP Id: rs397518466

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10180410A>G , CM000678.2:g.10180410A>G GRCh38
NC_000016.9:g.10274267A>G , CM000678.1:g.10274267A>G GRCh37
NC_000016.8:g.10181768A>G NCBI36
NG_011812.1:g.7345T>C
NG_011812.2:g.7345T>C

Transcript Alleles

HGVS Amino-acid change
NM_000833.4:c.2T>C VV
NM_001134407.2:c.2T>C VV
NM_001134408.2:c.2T>C VV
XM_011522461.1:c.2T>C
XM_011522461.3:c.2T>C
XM_017023172.1:c.158T>C XP_016878661.1:p.Met53Thr
XM_017023173.1:c.158T>C XP_016878662.1:p.Met53Thr
NM_001134407.3:c.2T>C VV MANE Preferred
NM_000833.5:c.2T>C VV
ENST00000330684.3:c.2T>C
ENST00000396573.6:c.2T>C
ENST00000562109.5:c.2T>C
ENST00000566665.1:n.403T>C