Canonical Allele Identifier: CA2318945636
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032578826
gnomAD v4: 19-3595424-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595424C>A , CM000681.2:g.3595424C>A GRCh38
NC_000019.9:g.3595422C>A , CM000681.1:g.3595422C>A GRCh37
NC_000019.8:g.3546422C>A NCBI36
NG_013363.1:g.16410G>T , LRG_578:g.16410G>T
NG_031943.1:g.14854C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*264G>T MANE Select ENSP00000364336.4:n.*264G>T
ENST00000375190.8:c.*264G>T ENSP00000364336.3:n.*264G>T
ENST00000411851.3:c.983+313G>T ENSP00000393333.2:n.983+313G>T
ENST00000589966.1:c.*127G>T ENSP00000468145.1:n.*127G>T
NM_001060.5:c.*264G>T , LRG_578t1:c.*264G>T NP_001051.1:n.*264G>T
NM_201636.2:c.983+313G>T NP_963998.2:n.983+313G>T
NM_001060.6:c.*264G>T MANE Select NP_001051.1:n.*264G>T
NM_201636.3:c.983+313G>T NP_963998.2:n.983+313G>T