Canonical Allele Identifier: CA322111530

Linked Data

dbSNP Id: rs746522569

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941428T>C , CM000684.2:g.19941428T>C GRCh38
NC_000022.10:g.19928951T>C , CM000684.1:g.19928951T>C GRCh37
NC_000022.9:g.18308951T>C NCBI36
NG_011526.1:g.4689T>C
NG_011835.1:g.5409A>G , LRG_417:g.5409A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+273A>G (TXNRD2) MANE Select ENSP00000383365.1:n.103+273A>G
ENST00000676678.1:c.-239T>C (COMT) ENSP00000503719.1:n.-239T>C
ENST00000334363.14:c.103+273A>G (TXNRD2) ENSP00000334451.9:n.103+273A>G
ENST00000400519.6:c.103+273A>G (TXNRD2) ENSP00000383363.1:n.103+273A>G
ENST00000400521.6:c.103+273A>G (TXNRD2) ENSP00000383365.1:n.103+273A>G
ENST00000400525.6:c.103+273A>G (TXNRD2) ENSP00000383369.3:n.103+273A>G
ENST00000474308.5:c.103+273A>G (TXNRD2) ENSP00000485665.1:n.103+273A>G
ENST00000496729.2:n.108+273A>G (TXNRD2)
NM_001282512.1:c.103+273A>G (TXNRD2) NP_001269441.1:n.103+273A>G
NM_006440.4:c.103+273A>G (TXNRD2) NP_006431.2:n.103+273A>G
NM_001282512.2:c.103+273A>G (TXNRD2) NP_001269441.1:n.103+273A>G
NM_001352300.1:c.103+273A>G (TXNRD2) NP_001339229.1:n.103+273A>G
NR_147957.1:n.292+273A>G (TXNRD2)
NM_006440.5:c.103+273A>G (TXNRD2) MANE Select NP_006431.2:n.103+273A>G
NM_001282512.3:c.103+273A>G (TXNRD2) NP_001269441.1:n.103+273A>G
NM_001352300.2:c.103+273A>G (TXNRD2) NP_001339229.1:n.103+273A>G
NR_147957.2:n.118+273A>G (TXNRD2)