Canonical Allele Identifier: CA751471358
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs2075507

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19940569G>T , CM000684.2:g.19940569G>T GRCh38
NC_000022.10:g.19928092G>T , CM000684.1:g.19928092G>T GRCh37
NC_000022.9:g.18308092G>T NCBI36
NG_011526.1:g.3830G>T
NG_011835.1:g.6268C>A , LRG_417:g.6268C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+1132C>A MANE Select ENSP00000383365.1:n.103+1132C>A
ENST00000334363.14:c.103+1132C>A ENSP00000334451.9:n.103+1132C>A
ENST00000400519.6:c.103+1132C>A ENSP00000383363.1:n.103+1132C>A
ENST00000400521.6:c.103+1132C>A ENSP00000383365.1:n.103+1132C>A
ENST00000400525.6:c.103+1132C>A ENSP00000383369.3:n.103+1132C>A
ENST00000474308.5:c.103+1132C>A ENSP00000485665.1:n.103+1132C>A
ENST00000496729.2:n.108+1132C>A
NM_001282512.1:c.103+1132C>A NP_001269441.1:n.103+1132C>A
NM_006440.4:c.103+1132C>A NP_006431.2:n.103+1132C>A
NM_001282512.2:c.103+1132C>A NP_001269441.1:n.103+1132C>A
NM_001352300.1:c.103+1132C>A NP_001339229.1:n.103+1132C>A
NR_147957.1:n.292+1132C>A
NM_006440.5:c.103+1132C>A MANE Select NP_006431.2:n.103+1132C>A
NM_001282512.3:c.103+1132C>A NP_001269441.1:n.103+1132C>A
NM_001352300.2:c.103+1132C>A NP_001339229.1:n.103+1132C>A
NR_147957.2:n.118+1132C>A