Canonical Allele Identifier: CA631504250
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1377671248
gnomAD v2: 19-3595356-G-A
gnomAD v4: 19-3595358-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595358G>A , CM000681.2:g.3595358G>A GRCh38
NC_000019.9:g.3595356G>A , CM000681.1:g.3595356G>A GRCh37
NC_000019.8:g.3546356G>A NCBI36
NG_013363.1:g.16476C>T , LRG_578:g.16476C>T
NG_031943.1:g.14788G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*330C>T MANE Select ENSP00000364336.4:n.*330C>T
ENST00000375190.8:c.*330C>T ENSP00000364336.3:n.*330C>T
ENST00000411851.3:c.984-282C>T ENSP00000393333.2:n.984-282C>T
ENST00000589966.1:c.*193C>T ENSP00000468145.1:n.*193C>T
NM_001060.5:c.*330C>T , LRG_578t1:c.*330C>T NP_001051.1:n.*330C>T
NM_201636.2:c.984-282C>T NP_963998.2:n.984-282C>T
NM_001060.6:c.*330C>T MANE Select NP_001051.1:n.*330C>T
NM_201636.3:c.984-282C>T NP_963998.2:n.984-282C>T