LDH info

Canonical Allele Identifier: CA14963943
Gene: TXNRD2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2020917

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941361C>T , CM000684.2:g.19941361C>T GRCh38
NC_000022.10:g.19928884C>T , CM000684.1:g.19928884C>T GRCh37
NC_000022.9:g.18308884C>T NCBI36
NG_011526.1:g.4622C>T
NG_011835.1:g.5476G>A , LRG_417:g.5476G>A

Transcript Alleles

HGVS Amino-acid change
NM_001282512.1:c.103+340G>A VV NP_001269441.1:p.=
NM_006440.4:c.103+340G>A VV NP_006431.2:p.=
NM_001282512.2:c.103+340G>A VV NP_001269441.1:p.=
NM_001352300.1:c.103+340G>A VV NP_001339229.1:p.=
NR_147957.1:n.292+340G>A
NM_006440.5:c.103+340G>A VV MANE Preferred NP_006431.2:p.=
NM_001282512.3:c.103+340G>A VV NP_001269441.1:p.=
NM_001352300.2:c.103+340G>A VV NP_001339229.1:p.=
NR_147957.2:n.118+340G>A
ENST00000334363.14:c.103+340G>A ENSP00000334451.9:p.=
ENST00000400519.6:n.103+340G>A ENSP00000383363.1:p.=
ENST00000400521.6:c.103+340G>A ENSP00000383365.1:p.=
ENST00000400525.6:c.103+340G>A ENSP00000383369.3:p.=
ENST00000474308.5:c.103+340G>A ENSP00000485665.1:p.=
ENST00000496729.2:n.108+340G>A