Canonical Allele Identifier: CA403331303

Gene: TBXA2R

Linked Data

• gnomAD v4: 19-3595919-C-A
• MyVariant Identifiers: chr19:g.3595917C>A (hg19) ; chr19:g.3595919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595919C>A , CM000681.2:g.3595919C>A	GRCh38
NC_000019.9:g.3595917C>A , CM000681.1:g.3595917C>A	GRCh37
NC_000019.8:g.3546917C>A	NCBI36
NG_013363.1:g.15915G>T , LRG_578:g.15915G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.801G>T MANE Select	ENSP00000364336.4:p.Gln267His
ENST00000375190.8:c.801G>T	ENSP00000364336.3:p.Gln267His
ENST00000411851.3:c.801G>T	ENSP00000393333.2:p.Gln267His
ENST00000589966.1:c.412G>T	ENSP00000468145.1:p.Asp138Tyr
NM_001060.5:c.801G>T , LRG_578t1:c.801G>T	NP_001051.1:p.Gln267His
NM_201636.2:c.801G>T	NP_963998.2:p.Gln267His
XM_011528214.1:c.801G>T	XP_011526516.1:p.Gln267His
XM_011528214.2:c.801G>T	XP_011526516.1:p.Gln267His
NM_001060.6:c.801G>T MANE Select	NP_001051.1:p.Gln267His
NM_201636.3:c.801G>T	NP_963998.2:p.Gln267His