LDH info

Canonical Allele Identifier: CA199157
Gene: CNGA3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9476
dbSNP Id: rs104893615

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396839G>A , CM000664.2:g.98396839G>A GRCh38
NC_000002.11:g.99013302G>A , CM000664.1:g.99013302G>A GRCh37
NC_000002.10:g.98379734G>A NCBI36
NG_009097.1:g.55685G>A

Transcript Alleles

HGVS Amino-acid change
NM_001079878.1:c.1615G>A VV NP_001073347.1:p.Gly539Arg
NM_001298.2:c.1669G>A VV NP_001289.1:p.Gly557Arg
XM_006712243.2:c.1780G>A XP_006712306.1:p.Gly594Arg
XM_011510554.1:c.1834G>A XP_011508856.1:p.Gly612Arg
XM_011510554.2:c.1834G>A XP_011508856.1:p.Gly612Arg
NM_001079878.2:c.1615G>A VV NP_001073347.1:p.Gly539Arg
NM_001298.3:c.1669G>A VV NP_001289.1:p.Gly557Arg
ENST00000272602.6:c.1669G>A ENSP00000272602.2:p.Gly557Arg
ENST00000393504.5:c.1669G>A ENSP00000377140.1:p.Gly557Arg
ENST00000409937.1:c.1681G>A ENSP00000386761.1:p.Gly561Arg
ENST00000436404.6:c.1615G>A ENSP00000410070.2:p.Gly539Arg