Canonical Allele Identifier: CA10104276

Gene: TXNRD2

Linked Data

• ClinVar Variation Id: 1936412
• ClinVar RCV Id: RCV002636403
• dbSNP Id: rs770945312
• ExAC: 22:19906502 G / A
• gnomAD v2: 22-19906502-G-A
• gnomAD v4: 22-19918979-G-A
• MyVariant Identifiers: chr22:g.19906502G>A (hg19) ; chr22:g.19918979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918979G>A , CM000684.2:g.19918979G>A	GRCh38
NC_000022.10:g.19906502G>A , CM000684.1:g.19906502G>A	GRCh37
NC_000022.9:g.18286502G>A	NCBI36
NG_011835.1:g.27858C>T , LRG_417:g.27858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.255C>T MANE Select	ENSP00000383365.1:p.Thr85=
ENST00000334363.14:c.255C>T	ENSP00000334451.9:p.Thr85=
ENST00000400518.5:c.165C>T	ENSP00000383362.1:p.Thr55=
ENST00000400519.6:c.252C>T	ENSP00000383363.1:p.Thr84=
ENST00000400521.6:c.255C>T	ENSP00000383365.1:p.Thr85=
ENST00000400525.6:c.186C>T	ENSP00000383369.3:p.Thr62=
ENST00000474308.5:c.198C>T	ENSP00000485665.1:p.Thr66=
ENST00000491939.6:c.159C>T	ENSP00000485543.1:p.Thr53=
ENST00000496729.2:n.260C>T
ENST00000542719.6:c.-34C>T	ENSP00000485128.2:n.-34C>T
NM_001282512.1:c.255C>T	NP_001269441.1:p.Thr85=
NM_006440.4:c.255C>T	NP_006431.2:p.Thr85=
NM_001282512.2:c.255C>T	NP_001269441.1:p.Thr85=
NM_001352300.1:c.252C>T	NP_001339229.1:p.Thr84=
NM_001352301.1:c.165C>T	NP_001339230.1:p.Thr55=
NM_001352302.1:c.-34C>T	NP_001339231.1:n.-34C>T
NM_001352303.1:c.159C>T	NP_001339232.1:p.Thr53=
NR_147957.1:n.387C>T
NM_006440.5:c.255C>T MANE Select	NP_006431.2:p.Thr85=
NM_001282512.3:c.255C>T	NP_001269441.1:p.Thr85=
NM_001352300.2:c.252C>T	NP_001339229.1:p.Thr84=
NR_147957.2:n.213C>T
NM_001352301.2:c.165C>T	NP_001339230.1:p.Thr55=
NM_001352302.2:c.-34C>T	NP_001339231.1:n.-34C>T
NM_001352303.2:c.159C>T	NP_001339232.1:p.Thr53=