Canonical Allele Identifier: CA2318945929
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595919C= , CM000681.2:g.3595919C= GRCh38
NC_000019.9:g.3595917C= , CM000681.1:g.3595917C= GRCh37
NC_000019.8:g.3546917C= NCBI36
NG_013363.1:g.15915G= , LRG_578:g.15915G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.801G= MANE Select ENSP00000364336.4:p.Gln267=
ENST00000375190.8:c.801G= ENSP00000364336.3:p.Gln267=
ENST00000411851.3:c.801G= ENSP00000393333.2:p.Gln267=
ENST00000589966.1:c.412G= ENSP00000468145.1:p.Asp138=
NM_001060.5:c.801G= , LRG_578t1:c.801G= NP_001051.1:p.Gln267=
NM_201636.2:c.801G= NP_963998.2:p.Gln267=
XM_011528214.1:c.801G= XP_011526516.1:p.Gln267=
XM_011528214.2:c.801G= XP_011526516.1:p.Gln267=
NM_001060.6:c.801G= MANE Select NP_001051.1:p.Gln267=
NM_201636.3:c.801G= NP_963998.2:p.Gln267=