Canonical Allele Identifier: CA2318945662
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032579709

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595457dup , CM000681.2:g.3595457dup GRCh38
NC_000019.9:g.3595455dup , CM000681.1:g.3595455dup GRCh37
NC_000019.8:g.3546455dup NCBI36
NG_013363.1:g.16380dup , LRG_578:g.16380dup
NG_031943.1:g.14887dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*234dup MANE Select ENSP00000364336.4:n.*234dup
ENST00000375190.8:c.*234dup ENSP00000364336.3:n.*234dup
ENST00000411851.3:c.983+283dup ENSP00000393333.2:n.983+283dup
ENST00000589966.1:c.*97dup ENSP00000468145.1:n.*97dup
NM_001060.5:c.*234dup , LRG_578t1:c.*234dup NP_001051.1:n.*234dup
NM_201636.2:c.983+283dup NP_963998.2:n.983+283dup
NM_001060.6:c.*234dup MANE Select NP_001051.1:n.*234dup
NM_201636.3:c.983+283dup NP_963998.2:n.983+283dup