Canonical Allele Identifier: CA10210819
Gene: TXN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1280669
dbSNP Id: rs2281082

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36476703T>G , CM000684.2:g.36476703T>G GRCh38
NC_000022.10:g.36872750T>G , CM000684.1:g.36872750T>G GRCh37
NC_000022.9:g.35202696T>G NCBI36
NG_046718.1:g.9938A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216185.7:c.387+30A>C MANE Select ENSP00000216185.2:n.387+30A>C
ENST00000216185.6:c.387+30A>C ENSP00000216185.2:n.387+30A>C
ENST00000403313.5:c.387+30A>C ENSP00000385393.1:n.387+30A>C
ENST00000411915.1:c.387+30A>C ENSP00000409407.1:n.387+30A>C
ENST00000416967.1:c.81+30A>C ENSP00000469160.1:n.81+30A>C
ENST00000487725.1:n.367+30A>C
NM_012473.3:c.387+30A>C NP_036605.2:n.387+30A>C
XM_005261508.1:c.480+30A>C XP_005261565.1:n.480+30A>C
XM_006724226.1:c.387+30A>C XP_006724289.1:n.387+30A>C
XM_011530111.1:c.356+3872A>C XP_011528413.1:n.356+3872A>C
XM_011530111.3:c.356+3872A>C XP_011528413.1:n.356+3872A>C
NM_012473.4:c.387+30A>C MANE Select NP_036605.2:n.387+30A>C