Canonical Allele Identifier: CA881803571
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1323546666
gnomAD v3: 19-3595473-G-T
gnomAD v4: 19-3595473-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595473G>T , CM000681.2:g.3595473G>T GRCh38
NC_000019.9:g.3595471G>T , CM000681.1:g.3595471G>T GRCh37
NC_000019.8:g.3546471G>T NCBI36
NG_013363.1:g.16361C>A , LRG_578:g.16361C>A
NG_031943.1:g.14903G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*215C>A MANE Select ENSP00000364336.4:n.*215C>A
ENST00000375190.8:c.*215C>A ENSP00000364336.3:n.*215C>A
ENST00000411851.3:c.983+264C>A ENSP00000393333.2:n.983+264C>A
ENST00000589966.1:c.*78C>A ENSP00000468145.1:n.*78C>A
NM_001060.5:c.*215C>A , LRG_578t1:c.*215C>A NP_001051.1:n.*215C>A
NM_201636.2:c.983+264C>A NP_963998.2:n.983+264C>A
NM_001060.6:c.*215C>A MANE Select NP_001051.1:n.*215C>A
NM_201636.3:c.983+264C>A NP_963998.2:n.983+264C>A