Canonical Allele Identifier: CA2318945629
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595413T= , CM000681.2:g.3595413T= GRCh38
NC_000019.9:g.3595411T= , CM000681.1:g.3595411T= GRCh37
NC_000019.8:g.3546411T= NCBI36
NG_013363.1:g.16421A= , LRG_578:g.16421A=
NG_031943.1:g.14843T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*275A= MANE Select ENSP00000364336.4:n.*275A=
ENST00000375190.8:c.*275A= ENSP00000364336.3:n.*275A=
ENST00000411851.3:c.983+324A= ENSP00000393333.2:n.983+324A=
ENST00000589966.1:c.*138A= ENSP00000468145.1:n.*138A=
NM_001060.5:c.*275A= , LRG_578t1:c.*275A= NP_001051.1:n.*275A=
NM_201636.2:c.983+324A= NP_963998.2:n.983+324A=
NM_001060.6:c.*275A= MANE Select NP_001051.1:n.*275A=
NM_201636.3:c.983+324A= NP_963998.2:n.983+324A=