LDH info

Canonical Allele Identifier: CA121979
Gene: AVP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12221
ClinVar RCV Id: RCV000013005
dbSNP Id: rs121964893

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084614A>G , CM000682.2:g.3084614A>G GRCh38
NC_000020.10:g.3065260A>G , CM000682.1:g.3065260A>G GRCh37
NC_000020.9:g.3013260A>G NCBI36
NG_008663.1:g.5111T>C , LRG_715:g.5111T>C

Transcript Alleles

HGVS Amino-acid change
NM_000490.4:c.61T>C , LRG_715t1:c.61T>C NP_000481.2:p.Tyr21His
XM_011529267.1:c.61T>C XP_011527569.1:p.Tyr21His
XM_011529267.2:c.61T>C XP_011527569.1:p.Tyr21His
NM_000490.5:c.61T>C VV MANE Preferred NP_000481.2:p.Tyr21His
ENST00000380293.3:c.61T>C ENSP00000369647.3:p.Tyr21His