Canonical Allele Identifier: CA2318945590
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032577028
gnomAD v4: 19-3595369-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595369A>C , CM000681.2:g.3595369A>C GRCh38
NC_000019.9:g.3595367A>C , CM000681.1:g.3595367A>C GRCh37
NC_000019.8:g.3546367A>C NCBI36
NG_013363.1:g.16465T>G , LRG_578:g.16465T>G
NG_031943.1:g.14799A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*319T>G MANE Select ENSP00000364336.4:n.*319T>G
ENST00000375190.8:c.*319T>G ENSP00000364336.3:n.*319T>G
ENST00000411851.3:c.984-293T>G ENSP00000393333.2:n.984-293T>G
ENST00000589966.1:c.*182T>G ENSP00000468145.1:n.*182T>G
NM_001060.5:c.*319T>G , LRG_578t1:c.*319T>G NP_001051.1:n.*319T>G
NM_201636.2:c.984-293T>G NP_963998.2:n.984-293T>G
NM_001060.6:c.*319T>G MANE Select NP_001051.1:n.*319T>G
NM_201636.3:c.984-293T>G NP_963998.2:n.984-293T>G