Canonical Allele Identifier: CA513369064
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1940761258
MyVariant Identifiers: chr22:g.19906433T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918910T>C , CM000684.2:g.19918910T>C GRCh38
NC_000022.10:g.19906433T>C , CM000684.1:g.19906433T>C GRCh37
NC_000022.9:g.18286433T>C NCBI36
NG_011835.1:g.27927A>G , LRG_417:g.27927A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.324A>G MANE Select ENSP00000383365.1:p.Gln108=
ENST00000334363.14:c.324A>G ENSP00000334451.9:p.Gln108=
ENST00000400518.5:c.234A>G ENSP00000383362.1:p.Gln78=
ENST00000400519.6:c.321A>G ENSP00000383363.1:p.Gln107=
ENST00000400521.6:c.324A>G ENSP00000383365.1:p.Gln108=
ENST00000400525.6:c.255A>G ENSP00000383369.3:p.Gln85=
ENST00000474308.5:c.267A>G ENSP00000485665.1:p.Gln89=
ENST00000491939.6:c.228A>G ENSP00000485543.1:p.Gln76=
ENST00000496729.2:n.329A>G
ENST00000542719.6:c.36A>G ENSP00000485128.2:p.Gln12=
NM_001282512.1:c.324A>G NP_001269441.1:p.Gln108=
NM_006440.4:c.324A>G NP_006431.2:p.Gln108=
NM_001282512.2:c.324A>G NP_001269441.1:p.Gln108=
NM_001352300.1:c.321A>G NP_001339229.1:p.Gln107=
NM_001352301.1:c.234A>G NP_001339230.1:p.Gln78=
NM_001352302.1:c.36A>G NP_001339231.1:p.Gln12=
NM_001352303.1:c.228A>G NP_001339232.1:p.Gln76=
NR_147957.1:n.456A>G
NM_006440.5:c.324A>G MANE Select NP_006431.2:p.Gln108=
NM_001282512.3:c.324A>G NP_001269441.1:p.Gln108=
NM_001352300.2:c.321A>G NP_001339229.1:p.Gln107=
NR_147957.2:n.282A>G
NM_001352301.2:c.234A>G NP_001339230.1:p.Gln78=
NM_001352302.2:c.36A>G NP_001339231.1:p.Gln12=
NM_001352303.2:c.228A>G NP_001339232.1:p.Gln76=