Canonical Allele Identifier: CA2396090232

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1939284283

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19892024A>G , CM000684.2:g.19892024A>G	GRCh38
NC_000022.10:g.19879547A>G , CM000684.1:g.19879547A>G	GRCh37
NC_000022.9:g.18259547A>G	NCBI36
NG_011835.1:g.54813T>C , LRG_417:g.54813T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.949+3383T>C MANE Select	ENSP00000383365.1:n.949+3383T>C
ENST00000400518.5:c.859+3383T>C	ENSP00000383362.1:n.859+3383T>C
ENST00000400519.6:c.946+3383T>C	ENSP00000383363.1:n.946+3383T>C
ENST00000400521.6:c.949+3383T>C	ENSP00000383365.1:n.949+3383T>C
ENST00000400525.6:c.880+3383T>C	ENSP00000383369.3:n.880+3383T>C
ENST00000474308.5:c.892+3383T>C	ENSP00000485665.1:n.892+3383T>C
ENST00000494454.5:n.1023+3383T>C
ENST00000542719.6:c.661+3383T>C	ENSP00000485128.2:n.661+3383T>C
ENST00000634537.1:c.178+3383T>C	ENSP00000489208.1:n.178+3383T>C
ENST00000635155.1:n.536-264T>C
NM_006440.4:c.949+3383T>C	NP_006431.2:n.949+3383T>C
NM_001352300.1:c.946+3383T>C	NP_001339229.1:n.946+3383T>C
NM_001352301.1:c.859+3383T>C	NP_001339230.1:n.859+3383T>C
NM_001352302.1:c.661+3383T>C	NP_001339231.1:n.661+3383T>C
NR_147957.1:n.1081+3383T>C
NM_006440.5:c.949+3383T>C MANE Select	NP_006431.2:n.949+3383T>C
NM_001352300.2:c.946+3383T>C	NP_001339229.1:n.946+3383T>C
NR_147957.2:n.907+3383T>C
NM_001352301.2:c.859+3383T>C	NP_001339230.1:n.859+3383T>C
NM_001352302.2:c.661+3383T>C	NP_001339231.1:n.661+3383T>C