Canonical Allele Identifier: CA2318945631
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595417T= , CM000681.2:g.3595417T= GRCh38
NC_000019.9:g.3595415T= , CM000681.1:g.3595415T= GRCh37
NC_000019.8:g.3546415T= NCBI36
NG_013363.1:g.16417A= , LRG_578:g.16417A=
NG_031943.1:g.14847T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*271A= MANE Select ENSP00000364336.4:n.*271A=
ENST00000375190.8:c.*271A= ENSP00000364336.3:n.*271A=
ENST00000411851.3:c.983+320A= ENSP00000393333.2:n.983+320A=
ENST00000589966.1:c.*134A= ENSP00000468145.1:n.*134A=
NM_001060.5:c.*271A= , LRG_578t1:c.*271A= NP_001051.1:n.*271A=
NM_201636.2:c.983+320A= NP_963998.2:n.983+320A=
NM_001060.6:c.*271A= MANE Select NP_001051.1:n.*271A=
NM_201636.3:c.983+320A= NP_963998.2:n.983+320A=