Canonical Allele Identifier: CA2318945616
Gene: TBXA2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595401A= , CM000681.2:g.3595401A= GRCh38
NC_000019.9:g.3595399A= , CM000681.1:g.3595399A= GRCh37
NC_000019.8:g.3546399A= NCBI36
NG_013363.1:g.16433T= , LRG_578:g.16433T=
NG_031943.1:g.14831A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*287T= MANE Select ENSP00000364336.4:n.*287T=
ENST00000375190.8:c.*287T= ENSP00000364336.3:n.*287T=
ENST00000411851.3:c.984-325T= ENSP00000393333.2:n.984-325T=
ENST00000589966.1:c.*150T= ENSP00000468145.1:n.*150T=
NM_001060.5:c.*287T= , LRG_578t1:c.*287T= NP_001051.1:n.*287T=
NM_201636.2:c.984-325T= NP_963998.2:n.984-325T=
NM_001060.6:c.*287T= MANE Select NP_001051.1:n.*287T=
NM_201636.3:c.984-325T= NP_963998.2:n.984-325T=
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