Canonical Allele Identifier: CA322105573

Gene: TXNRD2

Linked Data

• dbSNP Id: rs973303265
• gnomAD v3: 22-19918816-G-C
• gnomAD v4: 22-19918816-G-C
• MyVariant Identifiers: chr22:g.19906339G>C (hg19) ; chr22:g.19918816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918816G>C , CM000684.2:g.19918816G>C	GRCh38
NC_000022.10:g.19906339G>C , CM000684.1:g.19906339G>C	GRCh37
NC_000022.9:g.18286339G>C	NCBI36
NG_011835.1:g.28021C>G , LRG_417:g.28021C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.374+44C>G MANE Select	ENSP00000383365.1:n.374+44C>G
ENST00000334363.14:c.374+44C>G	ENSP00000334451.9:n.374+44C>G
ENST00000400518.5:c.284+44C>G	ENSP00000383362.1:n.284+44C>G
ENST00000400519.6:c.371+44C>G	ENSP00000383363.1:n.371+44C>G
ENST00000400521.6:c.374+44C>G	ENSP00000383365.1:n.374+44C>G
ENST00000400525.6:c.305+44C>G	ENSP00000383369.3:n.305+44C>G
ENST00000474308.5:c.317+44C>G	ENSP00000485665.1:n.317+44C>G
ENST00000491939.6:c.278+44C>G	ENSP00000485543.1:n.278+44C>G
ENST00000496729.2:n.379+44C>G
ENST00000542719.6:c.86+44C>G	ENSP00000485128.2:n.86+44C>G
NM_001282512.1:c.374+44C>G	NP_001269441.1:n.374+44C>G
NM_006440.4:c.374+44C>G	NP_006431.2:n.374+44C>G
NM_001282512.2:c.374+44C>G	NP_001269441.1:n.374+44C>G
NM_001352300.1:c.371+44C>G	NP_001339229.1:n.371+44C>G
NM_001352301.1:c.284+44C>G	NP_001339230.1:n.284+44C>G
NM_001352302.1:c.86+44C>G	NP_001339231.1:n.86+44C>G
NM_001352303.1:c.278+44C>G	NP_001339232.1:n.278+44C>G
NR_147957.1:n.506+44C>G
NM_006440.5:c.374+44C>G MANE Select	NP_006431.2:n.374+44C>G
NM_001282512.3:c.374+44C>G	NP_001269441.1:n.374+44C>G
NM_001352300.2:c.371+44C>G	NP_001339229.1:n.371+44C>G
NR_147957.2:n.332+44C>G
NM_001352301.2:c.284+44C>G	NP_001339230.1:n.284+44C>G
NM_001352302.2:c.86+44C>G	NP_001339231.1:n.86+44C>G
NM_001352303.2:c.278+44C>G	NP_001339232.1:n.278+44C>G