Canonical Allele Identifier: CA2318945730
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595596C= , CM000681.2:g.3595596C= GRCh38
NC_000019.9:g.3595594C= , CM000681.1:g.3595594C= GRCh37
NC_000019.8:g.3546594C= NCBI36
NG_013363.1:g.16238G= , LRG_578:g.16238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*92G= MANE Select ENSP00000364336.4:n.*92G=
ENST00000375190.8:c.*92G= ENSP00000364336.3:n.*92G=
ENST00000411851.3:c.983+141G= ENSP00000393333.2:n.983+141G=
ENST00000589966.1:c.735G= ENSP00000468145.1:p.Gly245=
NM_001060.5:c.*92G= , LRG_578t1:c.*92G= NP_001051.1:n.*92G=
NM_201636.2:c.983+141G= NP_963998.2:n.983+141G=
XM_011528214.2:c.*92G= XP_011526516.1:n.*92G=
NM_001060.6:c.*92G= MANE Select NP_001051.1:n.*92G=
NM_201636.3:c.983+141G= NP_963998.2:n.983+141G=