Canonical Allele Identifier: CA2318945632
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595419C= , CM000681.2:g.3595419C= GRCh38
NC_000019.9:g.3595417C= , CM000681.1:g.3595417C= GRCh37
NC_000019.8:g.3546417C= NCBI36
NG_013363.1:g.16415G= , LRG_578:g.16415G=
NG_031943.1:g.14849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*269G= MANE Select ENSP00000364336.4:n.*269G=
ENST00000375190.8:c.*269G= ENSP00000364336.3:n.*269G=
ENST00000411851.3:c.983+318G= ENSP00000393333.2:n.983+318G=
ENST00000589966.1:c.*132G= ENSP00000468145.1:n.*132G=
NM_001060.5:c.*269G= , LRG_578t1:c.*269G= NP_001051.1:n.*269G=
NM_201636.2:c.983+318G= NP_963998.2:n.983+318G=
NM_001060.6:c.*269G= MANE Select NP_001051.1:n.*269G=
NM_201636.3:c.983+318G= NP_963998.2:n.983+318G=