Canonical Allele Identifier: CA403331139

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1381809178
• gnomAD v2: 19-3595882-G-T
• gnomAD v4: 19-3595884-G-T
• MyVariant Identifiers: chr19:g.3595882G>T (hg19) ; chr19:g.3595884G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595884G>T , CM000681.2:g.3595884G>T	GRCh38
NC_000019.9:g.3595882G>T , CM000681.1:g.3595882G>T	GRCh37
NC_000019.8:g.3546882G>T	NCBI36
NG_013363.1:g.15950C>A , LRG_578:g.15950C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.836C>A MANE Select	ENSP00000364336.4:p.Ala279Asp
ENST00000375190.8:c.836C>A	ENSP00000364336.3:p.Ala279Asp
ENST00000411851.3:c.836C>A	ENSP00000393333.2:p.Ala279Asp
ENST00000589966.1:c.447C>A	ENSP00000468145.1:p.Arg149=
NM_001060.5:c.836C>A , LRG_578t1:c.836C>A	NP_001051.1:p.Ala279Asp
NM_201636.2:c.836C>A	NP_963998.2:p.Ala279Asp
XM_011528214.1:c.836C>A	XP_011526516.1:p.Ala279Asp
XM_011528214.2:c.836C>A	XP_011526516.1:p.Ala279Asp
NM_001060.6:c.836C>A MANE Select	NP_001051.1:p.Ala279Asp
NM_201636.3:c.836C>A	NP_963998.2:p.Ala279Asp