Canonical Allele Identifier: CA2318945627
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032578511

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595408T>A , CM000681.2:g.3595408T>A GRCh38
NC_000019.9:g.3595406T>A , CM000681.1:g.3595406T>A GRCh37
NC_000019.8:g.3546406T>A NCBI36
NG_013363.1:g.16426A>T , LRG_578:g.16426A>T
NG_031943.1:g.14838T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*280A>T MANE Select ENSP00000364336.4:n.*280A>T
ENST00000375190.8:c.*280A>T ENSP00000364336.3:n.*280A>T
ENST00000411851.3:c.983+329A>T ENSP00000393333.2:n.983+329A>T
ENST00000589966.1:c.*143A>T ENSP00000468145.1:n.*143A>T
NM_001060.5:c.*280A>T , LRG_578t1:c.*280A>T NP_001051.1:n.*280A>T
NM_201636.2:c.983+329A>T NP_963998.2:n.983+329A>T
NM_001060.6:c.*280A>T MANE Select NP_001051.1:n.*280A>T
NM_201636.3:c.983+329A>T NP_963998.2:n.983+329A>T