Canonical Allele Identifier: CA2318945626
Gene: TBXA2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595408T= , CM000681.2:g.3595408T= GRCh38
NC_000019.9:g.3595406T= , CM000681.1:g.3595406T= GRCh37
NC_000019.8:g.3546406T= NCBI36
NG_013363.1:g.16426A= , LRG_578:g.16426A=
NG_031943.1:g.14838T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*280A= MANE Select ENSP00000364336.4:n.*280A=
ENST00000375190.8:c.*280A= ENSP00000364336.3:n.*280A=
ENST00000411851.3:c.983+329A= ENSP00000393333.2:n.983+329A=
ENST00000589966.1:c.*143A= ENSP00000468145.1:n.*143A=
NM_001060.5:c.*280A= , LRG_578t1:c.*280A= NP_001051.1:n.*280A=
NM_201636.2:c.983+329A= NP_963998.2:n.983+329A=
NM_001060.6:c.*280A= MANE Select NP_001051.1:n.*280A=
NM_201636.3:c.983+329A= NP_963998.2:n.983+329A=
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