Canonical Allele Identifier: CA2396114875

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1601499240

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941182A>C , CM000684.2:g.19941182A>C	GRCh38
NC_000022.10:g.19928705A>C , CM000684.1:g.19928705A>C	GRCh37
NC_000022.9:g.18308705A>C	NCBI36
NG_011526.1:g.4443A>C
NG_011835.1:g.5655T>G , LRG_417:g.5655T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+519T>G MANE Select	ENSP00000383365.1:n.103+519T>G
ENST00000334363.14:c.103+519T>G	ENSP00000334451.9:n.103+519T>G
ENST00000400519.6:c.103+519T>G	ENSP00000383363.1:n.103+519T>G
ENST00000400521.6:c.103+519T>G	ENSP00000383365.1:n.103+519T>G
ENST00000400525.6:c.103+519T>G	ENSP00000383369.3:n.103+519T>G
ENST00000474308.5:c.103+519T>G	ENSP00000485665.1:n.103+519T>G
ENST00000496729.2:n.108+519T>G
NM_001282512.1:c.103+519T>G	NP_001269441.1:n.103+519T>G
NM_006440.4:c.103+519T>G	NP_006431.2:n.103+519T>G
NM_001282512.2:c.103+519T>G	NP_001269441.1:n.103+519T>G
NM_001352300.1:c.103+519T>G	NP_001339229.1:n.103+519T>G
NR_147957.1:n.292+519T>G
NM_006440.5:c.103+519T>G MANE Select	NP_006431.2:n.103+519T>G
NM_001282512.3:c.103+519T>G	NP_001269441.1:n.103+519T>G
NM_001352300.2:c.103+519T>G	NP_001339229.1:n.103+519T>G
NR_147957.2:n.118+519T>G