Canonical Allele Identifier: CA2318945628
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595412A= , CM000681.2:g.3595412A= GRCh38
NC_000019.9:g.3595410A= , CM000681.1:g.3595410A= GRCh37
NC_000019.8:g.3546410A= NCBI36
NG_013363.1:g.16422T= , LRG_578:g.16422T=
NG_031943.1:g.14842A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*276T= MANE Select ENSP00000364336.4:n.*276T=
ENST00000375190.8:c.*276T= ENSP00000364336.3:n.*276T=
ENST00000411851.3:c.983+325T= ENSP00000393333.2:n.983+325T=
ENST00000589966.1:c.*139T= ENSP00000468145.1:n.*139T=
NM_001060.5:c.*276T= , LRG_578t1:c.*276T= NP_001051.1:n.*276T=
NM_201636.2:c.983+325T= NP_963998.2:n.983+325T=
NM_001060.6:c.*276T= MANE Select NP_001051.1:n.*276T=
NM_201636.3:c.983+325T= NP_963998.2:n.983+325T=