Canonical Allele Identifier: CA881803962
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1229635051

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595752_3595762del , CM000681.2:g.3595752_3595762del GRCh38
NC_000019.9:g.3595750_3595760del , CM000681.1:g.3595750_3595760del GRCh37
NC_000019.8:g.3546750_3546760del NCBI36
NG_013363.1:g.16076_16086del , LRG_578:g.16076_16086del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.962_972del MANE Select ENSP00000364336.4:p.Pro321HisfsTer?
ENST00000375190.8:c.962_972del ENSP00000364336.3:p.Pro321HisfsTer?
ENST00000411851.3:c.962_972del ENSP00000393333.2:p.Pro321HisfsTer?
ENST00000589966.1:c.573_583del ENSP00000468145.1:p.Ser192ProfsTer?
NM_001060.5:c.962_972del , LRG_578t1:c.962_972del NP_001051.1:p.Pro321HisfsTer?
NM_201636.2:c.962_972del NP_963998.2:p.Pro321HisfsTer?
XM_011528214.1:c.962_972del XP_011526516.1:p.Pro321HisfsTer?
XM_011528214.2:c.962_972del XP_011526516.1:p.Pro321HisfsTer?
NM_001060.6:c.962_972del MANE Select NP_001051.1:p.Pro321HisfsTer?
NM_201636.3:c.962_972del NP_963998.2:p.Pro321HisfsTer?