Canonical Allele Identifier: CA2318945657
Gene: TBXA2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595447C= , CM000681.2:g.3595447C= GRCh38
NC_000019.9:g.3595445C= , CM000681.1:g.3595445C= GRCh37
NC_000019.8:g.3546445C= NCBI36
NG_013363.1:g.16387G= , LRG_578:g.16387G=
NG_031943.1:g.14877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*241G= MANE Select ENSP00000364336.4:n.*241G=
ENST00000375190.8:c.*241G= ENSP00000364336.3:n.*241G=
ENST00000411851.3:c.983+290G= ENSP00000393333.2:n.983+290G=
ENST00000589966.1:c.*104G= ENSP00000468145.1:n.*104G=
NM_001060.5:c.*241G= , LRG_578t1:c.*241G= NP_001051.1:n.*241G=
NM_201636.2:c.983+290G= NP_963998.2:n.983+290G=
NM_001060.6:c.*241G= MANE Select NP_001051.1:n.*241G=
NM_201636.3:c.983+290G= NP_963998.2:n.983+290G=
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