Canonical Allele Identifier: CA2584493735
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595489-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595489G>A , CM000681.2:g.3595489G>A GRCh38
NC_000019.9:g.3595487G>A , CM000681.1:g.3595487G>A GRCh37
NC_000019.8:g.3546487G>A NCBI36
NG_013363.1:g.16345C>T , LRG_578:g.16345C>T
NG_031943.1:g.14919G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*199C>T MANE Select ENSP00000364336.4:n.*199C>T
ENST00000375190.8:c.*199C>T ENSP00000364336.3:n.*199C>T
ENST00000411851.3:c.983+248C>T ENSP00000393333.2:n.983+248C>T
ENST00000589966.1:c.*62C>T ENSP00000468145.1:n.*62C>T
NM_001060.5:c.*199C>T , LRG_578t1:c.*199C>T NP_001051.1:n.*199C>T
NM_201636.2:c.983+248C>T NP_963998.2:n.983+248C>T
NM_001060.6:c.*199C>T MANE Select NP_001051.1:n.*199C>T
NM_201636.3:c.983+248C>T NP_963998.2:n.983+248C>T