Canonical Allele Identifier: CA403330770
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1222106847
gnomAD v2: 19-3595826-T-A
gnomAD v4: 19-3595828-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595828T>A , CM000681.2:g.3595828T>A GRCh38
NC_000019.9:g.3595826T>A , CM000681.1:g.3595826T>A GRCh37
NC_000019.8:g.3546826T>A NCBI36
NG_013363.1:g.16006A>T , LRG_578:g.16006A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.892A>T MANE Select ENSP00000364336.4:p.Thr298Ser
ENST00000375190.8:c.892A>T ENSP00000364336.3:p.Thr298Ser
ENST00000411851.3:c.892A>T ENSP00000393333.2:p.Thr298Ser
ENST00000589966.1:c.503A>T ENSP00000468145.1:p.His168Leu
NM_001060.5:c.892A>T , LRG_578t1:c.892A>T NP_001051.1:p.Thr298Ser
NM_201636.2:c.892A>T NP_963998.2:p.Thr298Ser
XM_011528214.1:c.892A>T XP_011526516.1:p.Thr298Ser
XM_011528214.2:c.892A>T XP_011526516.1:p.Thr298Ser
NM_001060.6:c.892A>T MANE Select NP_001051.1:p.Thr298Ser
NM_201636.3:c.892A>T NP_963998.2:p.Thr298Ser