Canonical Allele Identifier: CA410693955

Gene: TXNRD2

Linked Data

• dbSNP Id: rs750564454
• gnomAD v2: 22-19906481-G-C
• gnomAD v3: 22-19918958-G-C
• gnomAD v4: 22-19918958-G-C
• MyVariant Identifiers: chr22:g.19906481G>C (hg19) ; chr22:g.19918958G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918958G>C , CM000684.2:g.19918958G>C	GRCh38
NC_000022.10:g.19906481G>C , CM000684.1:g.19906481G>C	GRCh37
NC_000022.9:g.18286481G>C	NCBI36
NG_011835.1:g.27879C>G , LRG_417:g.27879C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.276C>G MANE Select	ENSP00000383365.1:p.Ile92Met
ENST00000334363.14:c.276C>G	ENSP00000334451.9:p.Ile92Met
ENST00000400518.5:c.186C>G	ENSP00000383362.1:p.Ile62Met
ENST00000400519.6:c.273C>G	ENSP00000383363.1:p.Ile91Met
ENST00000400521.6:c.276C>G	ENSP00000383365.1:p.Ile92Met
ENST00000400525.6:c.207C>G	ENSP00000383369.3:p.Ile69Met
ENST00000474308.5:c.219C>G	ENSP00000485665.1:p.Ile73Met
ENST00000491939.6:c.180C>G	ENSP00000485543.1:p.Ile60Met
ENST00000496729.2:n.281C>G
ENST00000542719.6:c.-13C>G	ENSP00000485128.2:n.-13C>G
NM_001282512.1:c.276C>G	NP_001269441.1:p.Ile92Met
NM_006440.4:c.276C>G	NP_006431.2:p.Ile92Met
NM_001282512.2:c.276C>G	NP_001269441.1:p.Ile92Met
NM_001352300.1:c.273C>G	NP_001339229.1:p.Ile91Met
NM_001352301.1:c.186C>G	NP_001339230.1:p.Ile62Met
NM_001352302.1:c.-13C>G	NP_001339231.1:n.-13C>G
NM_001352303.1:c.180C>G	NP_001339232.1:p.Ile60Met
NR_147957.1:n.408C>G
NM_006440.5:c.276C>G MANE Select	NP_006431.2:p.Ile92Met
NM_001282512.3:c.276C>G	NP_001269441.1:p.Ile92Met
NM_001352300.2:c.273C>G	NP_001339229.1:p.Ile91Met
NR_147957.2:n.234C>G
NM_001352301.2:c.186C>G	NP_001339230.1:p.Ile62Met
NM_001352302.2:c.-13C>G	NP_001339231.1:n.-13C>G
NM_001352303.2:c.180C>G	NP_001339232.1:p.Ile60Met