Canonical Allele Identifier: CA304367764
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs956956539
gnomAD v4: 19-3595412-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595412A>G , CM000681.2:g.3595412A>G GRCh38
NC_000019.9:g.3595410A>G , CM000681.1:g.3595410A>G GRCh37
NC_000019.8:g.3546410A>G NCBI36
NG_013363.1:g.16422T>C , LRG_578:g.16422T>C
NG_031943.1:g.14842A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*276T>C MANE Select ENSP00000364336.4:n.*276T>C
ENST00000375190.8:c.*276T>C ENSP00000364336.3:n.*276T>C
ENST00000411851.3:c.983+325T>C ENSP00000393333.2:n.983+325T>C
ENST00000589966.1:c.*139T>C ENSP00000468145.1:n.*139T>C
NM_001060.5:c.*276T>C , LRG_578t1:c.*276T>C NP_001051.1:n.*276T>C
NM_201636.2:c.983+325T>C NP_963998.2:n.983+325T>C
NM_001060.6:c.*276T>C MANE Select NP_001051.1:n.*276T>C
NM_201636.3:c.983+325T>C NP_963998.2:n.983+325T>C