Canonical Allele Identifier: CA1024161241

Linked Data

dbSNP Id: rs1941709690

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941430G>T , CM000684.2:g.19941430G>T GRCh38
NC_000022.10:g.19928953G>T , CM000684.1:g.19928953G>T GRCh37
NC_000022.9:g.18308953G>T NCBI36
NG_011526.1:g.4691G>T
NG_011835.1:g.5407C>A , LRG_417:g.5407C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+271C>A (TXNRD2) MANE Select ENSP00000383365.1:n.103+271C>A
ENST00000676678.1:c.-237G>T (COMT) ENSP00000503719.1:n.-237G>T
ENST00000334363.14:c.103+271C>A (TXNRD2) ENSP00000334451.9:n.103+271C>A
ENST00000400519.6:c.103+271C>A (TXNRD2) ENSP00000383363.1:n.103+271C>A
ENST00000400521.6:c.103+271C>A (TXNRD2) ENSP00000383365.1:n.103+271C>A
ENST00000400525.6:c.103+271C>A (TXNRD2) ENSP00000383369.3:n.103+271C>A
ENST00000474308.5:c.103+271C>A (TXNRD2) ENSP00000485665.1:n.103+271C>A
ENST00000496729.2:n.108+271C>A (TXNRD2)
NM_001282512.1:c.103+271C>A (TXNRD2) NP_001269441.1:n.103+271C>A
NM_006440.4:c.103+271C>A (TXNRD2) NP_006431.2:n.103+271C>A
NM_001282512.2:c.103+271C>A (TXNRD2) NP_001269441.1:n.103+271C>A
NM_001352300.1:c.103+271C>A (TXNRD2) NP_001339229.1:n.103+271C>A
NR_147957.1:n.292+271C>A (TXNRD2)
NM_006440.5:c.103+271C>A (TXNRD2) MANE Select NP_006431.2:n.103+271C>A
NM_001282512.3:c.103+271C>A (TXNRD2) NP_001269441.1:n.103+271C>A
NM_001352300.2:c.103+271C>A (TXNRD2) NP_001339229.1:n.103+271C>A
NR_147957.2:n.118+271C>A (TXNRD2)