Canonical Allele Identifier: CA2318945598
Gene: TBXA2R HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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