Canonical Allele Identifier: CA881803560
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1260355818
gnomAD v3: 19-3595405-T-A
gnomAD v4: 19-3595405-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595405T>A , CM000681.2:g.3595405T>A GRCh38
NC_000019.9:g.3595403T>A , CM000681.1:g.3595403T>A GRCh37
NC_000019.8:g.3546403T>A NCBI36
NG_013363.1:g.16429A>T , LRG_578:g.16429A>T
NG_031943.1:g.14835T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*283A>T MANE Select ENSP00000364336.4:n.*283A>T
ENST00000375190.8:c.*283A>T ENSP00000364336.3:n.*283A>T
ENST00000411851.3:c.984-329A>T ENSP00000393333.2:n.984-329A>T
ENST00000589966.1:c.*146A>T ENSP00000468145.1:n.*146A>T
NM_001060.5:c.*283A>T , LRG_578t1:c.*283A>T NP_001051.1:n.*283A>T
NM_201636.2:c.984-329A>T NP_963998.2:n.984-329A>T
NM_001060.6:c.*283A>T MANE Select NP_001051.1:n.*283A>T
NM_201636.3:c.984-329A>T NP_963998.2:n.984-329A>T