Canonical Allele Identifier: CA322111505
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs965035318

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941352A>G , CM000684.2:g.19941352A>G GRCh38
NC_000022.10:g.19928875A>G , CM000684.1:g.19928875A>G GRCh37
NC_000022.9:g.18308875A>G NCBI36
NG_011526.1:g.4613A>G
NG_011835.1:g.5485T>C , LRG_417:g.5485T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+349T>C MANE Select ENSP00000383365.1:n.103+349T>C
ENST00000334363.14:c.103+349T>C ENSP00000334451.9:n.103+349T>C
ENST00000400519.6:c.103+349T>C ENSP00000383363.1:n.103+349T>C
ENST00000400521.6:c.103+349T>C ENSP00000383365.1:n.103+349T>C
ENST00000400525.6:c.103+349T>C ENSP00000383369.3:n.103+349T>C
ENST00000474308.5:c.103+349T>C ENSP00000485665.1:n.103+349T>C
ENST00000496729.2:n.108+349T>C
NM_001282512.1:c.103+349T>C NP_001269441.1:n.103+349T>C
NM_006440.4:c.103+349T>C NP_006431.2:n.103+349T>C
NM_001282512.2:c.103+349T>C NP_001269441.1:n.103+349T>C
NM_001352300.1:c.103+349T>C NP_001339229.1:n.103+349T>C
NR_147957.1:n.292+349T>C
NM_006440.5:c.103+349T>C MANE Select NP_006431.2:n.103+349T>C
NM_001282512.3:c.103+349T>C NP_001269441.1:n.103+349T>C
NM_001352300.2:c.103+349T>C NP_001339229.1:n.103+349T>C
NR_147957.2:n.118+349T>C