Canonical Allele Identifier: CA2318945577
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595350G= , CM000681.2:g.3595350G= GRCh38
NC_000019.9:g.3595348G= , CM000681.1:g.3595348G= GRCh37
NC_000019.8:g.3546348G= NCBI36
NG_013363.1:g.16484C= , LRG_578:g.16484C=
NG_031943.1:g.14780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*338C= MANE Select ENSP00000364336.4:n.*338C=
ENST00000375190.8:c.*338C= ENSP00000364336.3:n.*338C=
ENST00000411851.3:c.984-274C= ENSP00000393333.2:n.984-274C=
ENST00000589966.1:c.*201C= ENSP00000468145.1:n.*201C=
NM_001060.5:c.*338C= , LRG_578t1:c.*338C= NP_001051.1:n.*338C=
NM_201636.2:c.984-274C= NP_963998.2:n.984-274C=
NM_001060.6:c.*338C= MANE Select NP_001051.1:n.*338C=
NM_201636.3:c.984-274C= NP_963998.2:n.984-274C=