Canonical Allele Identifier: CA403331032
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595864T>G , CM000681.2:g.3595864T>G GRCh38
NC_000019.9:g.3595862T>G , CM000681.1:g.3595862T>G GRCh37
NC_000019.8:g.3546862T>G NCBI36
NG_013363.1:g.15970A>C , LRG_578:g.15970A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.856A>C MANE Select ENSP00000364336.4:p.Thr286Pro
ENST00000375190.8:c.856A>C ENSP00000364336.3:p.Thr286Pro
ENST00000411851.3:c.856A>C ENSP00000393333.2:p.Thr286Pro
ENST00000589966.1:c.467A>C ENSP00000468145.1:p.His156Pro
NM_001060.5:c.856A>C , LRG_578t1:c.856A>C NP_001051.1:p.Thr286Pro
NM_201636.2:c.856A>C NP_963998.2:p.Thr286Pro
XM_011528214.1:c.856A>C XP_011526516.1:p.Thr286Pro
XM_011528214.2:c.856A>C XP_011526516.1:p.Thr286Pro
NM_001060.6:c.856A>C MANE Select NP_001051.1:p.Thr286Pro
NM_201636.3:c.856A>C NP_963998.2:p.Thr286Pro