Canonical Allele Identifier: CA2318945775
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595677C= , CM000681.2:g.3595677C= GRCh38
NC_000019.9:g.3595675C= , CM000681.1:g.3595675C= GRCh37
NC_000019.8:g.3546675C= NCBI36
NG_013363.1:g.16157G= , LRG_578:g.16157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*11G= MANE Select ENSP00000364336.4:n.*11G=
ENST00000375190.8:c.*11G= ENSP00000364336.3:n.*11G=
ENST00000411851.3:c.983+60G= ENSP00000393333.2:n.983+60G=
ENST00000589966.1:c.654G= ENSP00000468145.1:p.Gln218=
NM_001060.5:c.*11G= , LRG_578t1:c.*11G= NP_001051.1:n.*11G=
NM_201636.2:c.983+60G= NP_963998.2:n.983+60G=
XM_011528214.1:c.*11G= XP_011526516.1:n.*11G=
XM_011528214.2:c.*11G= XP_011526516.1:n.*11G=
NM_001060.6:c.*11G= MANE Select NP_001051.1:n.*11G=
NM_201636.3:c.983+60G= NP_963998.2:n.983+60G=