Canonical Allele Identifier: CA2318945591
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595369A= , CM000681.2:g.3595369A= GRCh38
NC_000019.9:g.3595367A= , CM000681.1:g.3595367A= GRCh37
NC_000019.8:g.3546367A= NCBI36
NG_013363.1:g.16465T= , LRG_578:g.16465T=
NG_031943.1:g.14799A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*319T= MANE Select ENSP00000364336.4:n.*319T=
ENST00000375190.8:c.*319T= ENSP00000364336.3:n.*319T=
ENST00000411851.3:c.984-293T= ENSP00000393333.2:n.984-293T=
ENST00000589966.1:c.*182T= ENSP00000468145.1:n.*182T=
NM_001060.5:c.*319T= , LRG_578t1:c.*319T= NP_001051.1:n.*319T=
NM_201636.2:c.984-293T= NP_963998.2:n.984-293T=
NM_001060.6:c.*319T= MANE Select NP_001051.1:n.*319T=
NM_201636.3:c.984-293T= NP_963998.2:n.984-293T=