Canonical Allele Identifier: CA2318945805
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595711T= , CM000681.2:g.3595711T= GRCh38
NC_000019.9:g.3595709T= , CM000681.1:g.3595709T= GRCh37
NC_000019.8:g.3546709T= NCBI36
NG_013363.1:g.16123A= , LRG_578:g.16123A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.1009A= MANE Select ENSP00000364336.4:p.Thr337=
ENST00000375190.8:c.1009A= ENSP00000364336.3:p.Thr337=
ENST00000411851.3:c.983+26A= ENSP00000393333.2:n.983+26A=
ENST00000589966.1:c.620A= ENSP00000468145.1:p.His207=
NM_001060.5:c.1009A= , LRG_578t1:c.1009A= NP_001051.1:p.Thr337=
NM_201636.2:c.983+26A= NP_963998.2:n.983+26A=
XM_011528214.1:c.1009A= XP_011526516.1:p.Thr337=
XM_011528214.2:c.1009A= XP_011526516.1:p.Thr337=
NM_001060.6:c.1009A= MANE Select NP_001051.1:p.Thr337=
NM_201636.3:c.983+26A= NP_963998.2:n.983+26A=