Canonical Allele Identifier: CA322111320

Gene: TXNRD2

Linked Data

• dbSNP Id: rs544148153
• gnomAD v3: 22-19940545-G-T
• gnomAD v4: 22-19940545-G-T
• MyVariant Identifiers: chr22:g.19928068G>T (hg19) ; chr22:g.19940545G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940545G>T , CM000684.2:g.19940545G>T	GRCh38
NC_000022.10:g.19928068G>T , CM000684.1:g.19928068G>T	GRCh37
NC_000022.9:g.18308068G>T	NCBI36
NG_011526.1:g.3806G>T
NG_011835.1:g.6292C>A , LRG_417:g.6292C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+1156C>A MANE Select	ENSP00000383365.1:n.103+1156C>A
ENST00000334363.14:c.103+1156C>A	ENSP00000334451.9:n.103+1156C>A
ENST00000400519.6:c.103+1156C>A	ENSP00000383363.1:n.103+1156C>A
ENST00000400521.6:c.103+1156C>A	ENSP00000383365.1:n.103+1156C>A
ENST00000400525.6:c.103+1156C>A	ENSP00000383369.3:n.103+1156C>A
ENST00000474308.5:c.103+1156C>A	ENSP00000485665.1:n.103+1156C>A
ENST00000496729.2:n.108+1156C>A
NM_001282512.1:c.103+1156C>A	NP_001269441.1:n.103+1156C>A
NM_006440.4:c.103+1156C>A	NP_006431.2:n.103+1156C>A
NM_001282512.2:c.103+1156C>A	NP_001269441.1:n.103+1156C>A
NM_001352300.1:c.103+1156C>A	NP_001339229.1:n.103+1156C>A
NR_147957.1:n.292+1156C>A
NM_006440.5:c.103+1156C>A MANE Select	NP_006431.2:n.103+1156C>A
NM_001282512.3:c.103+1156C>A	NP_001269441.1:n.103+1156C>A
NM_001352300.2:c.103+1156C>A	NP_001339229.1:n.103+1156C>A
NR_147957.2:n.118+1156C>A