Canonical Allele Identifier: CA403330025
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595729A>T , CM000681.2:g.3595729A>T GRCh38
NC_000019.9:g.3595727A>T , CM000681.1:g.3595727A>T GRCh37
NC_000019.8:g.3546727A>T NCBI36
NG_013363.1:g.16105T>A , LRG_578:g.16105T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.991T>A MANE Select ENSP00000364336.4:p.Ser331Thr
ENST00000375190.8:c.991T>A ENSP00000364336.3:p.Ser331Thr
ENST00000411851.3:c.983+8T>A ENSP00000393333.2:n.983+8T>A
ENST00000589966.1:c.602T>A ENSP00000468145.1:p.Val201Asp
NM_001060.5:c.991T>A , LRG_578t1:c.991T>A NP_001051.1:p.Ser331Thr
NM_201636.2:c.983+8T>A NP_963998.2:n.983+8T>A
XM_011528214.1:c.991T>A XP_011526516.1:p.Ser331Thr
XM_011528214.2:c.991T>A XP_011526516.1:p.Ser331Thr
NM_001060.6:c.991T>A MANE Select NP_001051.1:p.Ser331Thr
NM_201636.3:c.983+8T>A NP_963998.2:n.983+8T>A