Canonical Allele Identifier: CA2318945665
Gene: TBXA2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595459G= , CM000681.2:g.3595459G= GRCh38
NC_000019.9:g.3595457G= , CM000681.1:g.3595457G= GRCh37
NC_000019.8:g.3546457G= NCBI36
NG_013363.1:g.16375C= , LRG_578:g.16375C=
NG_031943.1:g.14889G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*229C= MANE Select ENSP00000364336.4:n.*229C=
ENST00000375190.8:c.*229C= ENSP00000364336.3:n.*229C=
ENST00000411851.3:c.983+278C= ENSP00000393333.2:n.983+278C=
ENST00000589966.1:c.*92C= ENSP00000468145.1:n.*92C=
NM_001060.5:c.*229C= , LRG_578t1:c.*229C= NP_001051.1:n.*229C=
NM_201636.2:c.983+278C= NP_963998.2:n.983+278C=
NM_001060.6:c.*229C= MANE Select NP_001051.1:n.*229C=
NM_201636.3:c.983+278C= NP_963998.2:n.983+278C=
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