Canonical Allele Identifier: CA2318945890
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595863G= , CM000681.2:g.3595863G= GRCh38
NC_000019.9:g.3595861G= , CM000681.1:g.3595861G= GRCh37
NC_000019.8:g.3546861G= NCBI36
NG_013363.1:g.15971C= , LRG_578:g.15971C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.857C= MANE Select ENSP00000364336.4:p.Thr286=
ENST00000375190.8:c.857C= ENSP00000364336.3:p.Thr286=
ENST00000411851.3:c.857C= ENSP00000393333.2:p.Thr286=
ENST00000589966.1:c.468C= ENSP00000468145.1:p.His156=
NM_001060.5:c.857C= , LRG_578t1:c.857C= NP_001051.1:p.Thr286=
NM_201636.2:c.857C= NP_963998.2:p.Thr286=
XM_011528214.1:c.857C= XP_011526516.1:p.Thr286=
XM_011528214.2:c.857C= XP_011526516.1:p.Thr286=
NM_001060.6:c.857C= MANE Select NP_001051.1:p.Thr286=
NM_201636.3:c.857C= NP_963998.2:p.Thr286=