Canonical Allele Identifier: CA403330771
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595828-T-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.892A>G MANE Select ENSP00000364336.4:p.Thr298Ala
ENST00000375190.8:c.892A>G ENSP00000364336.3:p.Thr298Ala
ENST00000411851.3:c.892A>G ENSP00000393333.2:p.Thr298Ala
ENST00000589966.1:c.503A>G ENSP00000468145.1:p.His168Arg
NM_001060.5:c.892A>G , LRG_578t1:c.892A>G NP_001051.1:p.Thr298Ala
NM_201636.2:c.892A>G NP_963998.2:p.Thr298Ala
XM_011528214.1:c.892A>G XP_011526516.1:p.Thr298Ala
XM_011528214.2:c.892A>G XP_011526516.1:p.Thr298Ala
NM_001060.6:c.892A>G MANE Select NP_001051.1:p.Thr298Ala
NM_201636.3:c.892A>G NP_963998.2:p.Thr298Ala