Canonical Allele Identifier: CA992743527
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032577366
gnomAD v3: 19-3595375-T-A
gnomAD v4: 19-3595375-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595375T>A , CM000681.2:g.3595375T>A GRCh38
NC_000019.9:g.3595373T>A , CM000681.1:g.3595373T>A GRCh37
NC_000019.8:g.3546373T>A NCBI36
NG_013363.1:g.16459A>T , LRG_578:g.16459A>T
NG_031943.1:g.14805T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*313A>T MANE Select ENSP00000364336.4:n.*313A>T
ENST00000375190.8:c.*313A>T ENSP00000364336.3:n.*313A>T
ENST00000411851.3:c.984-299A>T ENSP00000393333.2:n.984-299A>T
ENST00000589966.1:c.*176A>T ENSP00000468145.1:n.*176A>T
NM_001060.5:c.*313A>T , LRG_578t1:c.*313A>T NP_001051.1:n.*313A>T
NM_201636.2:c.984-299A>T NP_963998.2:n.984-299A>T
NM_001060.6:c.*313A>T MANE Select NP_001051.1:n.*313A>T
NM_201636.3:c.984-299A>T NP_963998.2:n.984-299A>T