Canonical Allele Identifier: CA403330161

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1281185111
• gnomAD v2: 19-3595745-T-C
• MyVariant Identifiers: chr19:g.3595745T>C (hg19) ; chr19:g.3595747T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595747T>C , CM000681.2:g.3595747T>C	GRCh38
NC_000019.9:g.3595745T>C , CM000681.1:g.3595745T>C	GRCh37
NC_000019.8:g.3546745T>C	NCBI36
NG_013363.1:g.16087A>G , LRG_578:g.16087A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.973A>G MANE Select	ENSP00000364336.4:p.Thr325Ala
ENST00000375190.8:c.973A>G	ENSP00000364336.3:p.Thr325Ala
ENST00000411851.3:c.973A>G	ENSP00000393333.2:p.Thr325Ala
ENST00000589966.1:c.584A>G	ENSP00000468145.1:p.His195Arg
NM_001060.5:c.973A>G , LRG_578t1:c.973A>G	NP_001051.1:p.Thr325Ala
NM_201636.2:c.973A>G	NP_963998.2:p.Thr325Ala
XM_011528214.1:c.973A>G	XP_011526516.1:p.Thr325Ala
XM_011528214.2:c.973A>G	XP_011526516.1:p.Thr325Ala
NM_001060.6:c.973A>G MANE Select	NP_001051.1:p.Thr325Ala
NM_201636.3:c.973A>G	NP_963998.2:p.Thr325Ala