Canonical Allele Identifier: CA751471285

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1224195138
• MyVariant Identifiers: chr22:g.19927821C>T (hg19) ; chr22:g.19940298C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940298C>T , CM000684.2:g.19940298C>T	GRCh38
NC_000022.10:g.19927821C>T , CM000684.1:g.19927821C>T	GRCh37
NC_000022.9:g.18307821C>T	NCBI36
NG_011526.1:g.3559C>T
NG_011835.1:g.6539G>A , LRG_417:g.6539G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.103+1403G>A MANE Select	ENSP00000383365.1:n.103+1403G>A
ENST00000334363.14:c.103+1403G>A	ENSP00000334451.9:n.103+1403G>A
ENST00000400519.6:c.103+1403G>A	ENSP00000383363.1:n.103+1403G>A
ENST00000400521.6:c.103+1403G>A	ENSP00000383365.1:n.103+1403G>A
ENST00000400525.6:c.103+1403G>A	ENSP00000383369.3:n.103+1403G>A
ENST00000474308.5:c.103+1403G>A	ENSP00000485665.1:n.103+1403G>A
ENST00000496729.2:n.108+1403G>A
NM_001282512.1:c.103+1403G>A	NP_001269441.1:n.103+1403G>A
NM_006440.4:c.103+1403G>A	NP_006431.2:n.103+1403G>A
NM_001282512.2:c.103+1403G>A	NP_001269441.1:n.103+1403G>A
NM_001352300.1:c.103+1403G>A	NP_001339229.1:n.103+1403G>A
NR_147957.1:n.292+1403G>A
NM_006440.5:c.103+1403G>A MANE Select	NP_006431.2:n.103+1403G>A
NM_001282512.3:c.103+1403G>A	NP_001269441.1:n.103+1403G>A
NM_001352300.2:c.103+1403G>A	NP_001339229.1:n.103+1403G>A
NR_147957.2:n.118+1403G>A