LDH info

Canonical Allele Identifier: CA107742581
Gene: NR3C2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10519951

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148280467C>T , CM000666.2:g.148280467C>T GRCh38
NC_000004.11:g.149201619C>T , CM000666.1:g.149201619C>T GRCh37
NC_000004.10:g.149421069C>T NCBI36
NG_013350.1:g.167054G>A

Transcript Alleles

HGVS Amino-acid change
NM_000901.4:c.1758-20350G>A VV NP_000892.2:p.=
NM_001166104.1:c.1758-20350G>A VV NP_001159576.1:p.=
XM_011531975.1:c.1758-20350G>A XP_011530277.1:p.=
XM_011531976.1:c.1758-20350G>A XP_011530278.1:p.=
XM_011531977.1:c.1758-20350G>A XP_011530279.1:p.=
XM_011531978.1:c.1758-20350G>A XP_011530280.1:p.=
NM_001354819.1:c.1758-20350G>A VV NP_001341748.1:p.=
NR_148974.1:n.2121-20350G>A
XM_011531978.2:c.1758-20350G>A XP_011530280.1:p.=
NM_000901.5:c.1758-20350G>A VV MANE Preferred NP_000892.2:p.=
NM_001166104.2:c.1758-20350G>A VV NP_001159576.1:p.=
NR_148974.2:n.2015-20350G>A
ENST00000342437.8:c.1758-20350G>A ENSP00000343907.4:p.=
ENST00000344721.8:c.1758-20350G>A ENSP00000341390.4:p.=
ENST00000358102.7:c.1758-20350G>A ENSP00000350815.3:p.=
ENST00000504753.1:n.207-20350G>A
ENST00000511528.1:n.1758-20350G>A ENSP00000421481.1:p.=
ENST00000512865.5:c.1758-20350G>A ENSP00000423510.1:p.=
ENST00000625323.2:c.1758-20350G>A ENSP00000486719.1:p.=