Canonical Allele Identifier: CA403331289

Gene: TBXA2R

Linked Data

• gnomAD v4: 19-3595916-T-A
• MyVariant Identifiers: chr19:g.3595914T>A (hg19) ; chr19:g.3595916T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595916T>A , CM000681.2:g.3595916T>A	GRCh38
NC_000019.9:g.3595914T>A , CM000681.1:g.3595914T>A	GRCh37
NC_000019.8:g.3546914T>A	NCBI36
NG_013363.1:g.15918A>T , LRG_578:g.15918A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.804A>T MANE Select	ENSP00000364336.4:p.Thr268=
ENST00000375190.8:c.804A>T	ENSP00000364336.3:p.Thr268=
ENST00000411851.3:c.804A>T	ENSP00000393333.2:p.Thr268=
ENST00000589966.1:c.415A>T	ENSP00000468145.1:p.Ser139Cys
NM_001060.5:c.804A>T , LRG_578t1:c.804A>T	NP_001051.1:p.Thr268=
NM_201636.2:c.804A>T	NP_963998.2:p.Thr268=
XM_011528214.1:c.804A>T	XP_011526516.1:p.Thr268=
XM_011528214.2:c.804A>T	XP_011526516.1:p.Thr268=
NM_001060.6:c.804A>T MANE Select	NP_001051.1:p.Thr268=
NM_201636.3:c.804A>T	NP_963998.2:p.Thr268=