Canonical Allele Identifier: CA2318945579
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595355G= , CM000681.2:g.3595355G= GRCh38
NC_000019.9:g.3595353G= , CM000681.1:g.3595353G= GRCh37
NC_000019.8:g.3546353G= NCBI36
NG_013363.1:g.16479C= , LRG_578:g.16479C=
NG_031943.1:g.14785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*333C= MANE Select ENSP00000364336.4:n.*333C=
ENST00000375190.8:c.*333C= ENSP00000364336.3:n.*333C=
ENST00000411851.3:c.984-279C= ENSP00000393333.2:n.984-279C=
ENST00000589966.1:c.*196C= ENSP00000468145.1:n.*196C=
NM_001060.5:c.*333C= , LRG_578t1:c.*333C= NP_001051.1:n.*333C=
NM_201636.2:c.984-279C= NP_963998.2:n.984-279C=
NM_001060.6:c.*333C= MANE Select NP_001051.1:n.*333C=
NM_201636.3:c.984-279C= NP_963998.2:n.984-279C=