Canonical Allele Identifier: CA992743556
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032578183
gnomAD v3: 19-3595402-C-A
gnomAD v4: 19-3595402-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595402C>A , CM000681.2:g.3595402C>A GRCh38
NC_000019.9:g.3595400C>A , CM000681.1:g.3595400C>A GRCh37
NC_000019.8:g.3546400C>A NCBI36
NG_013363.1:g.16432G>T , LRG_578:g.16432G>T
NG_031943.1:g.14832C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*286G>T MANE Select ENSP00000364336.4:n.*286G>T
ENST00000375190.8:c.*286G>T ENSP00000364336.3:n.*286G>T
ENST00000411851.3:c.984-326G>T ENSP00000393333.2:n.984-326G>T
ENST00000589966.1:c.*149G>T ENSP00000468145.1:n.*149G>T
NM_001060.5:c.*286G>T , LRG_578t1:c.*286G>T NP_001051.1:n.*286G>T
NM_201636.2:c.984-326G>T NP_963998.2:n.984-326G>T
NM_001060.6:c.*286G>T MANE Select NP_001051.1:n.*286G>T
NM_201636.3:c.984-326G>T NP_963998.2:n.984-326G>T