Canonical Allele Identifier: CA2318945618
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595402C= , CM000681.2:g.3595402C= GRCh38
NC_000019.9:g.3595400C= , CM000681.1:g.3595400C= GRCh37
NC_000019.8:g.3546400C= NCBI36
NG_013363.1:g.16432G= , LRG_578:g.16432G=
NG_031943.1:g.14832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*286G= MANE Select ENSP00000364336.4:n.*286G=
ENST00000375190.8:c.*286G= ENSP00000364336.3:n.*286G=
ENST00000411851.3:c.984-326G= ENSP00000393333.2:n.984-326G=
ENST00000589966.1:c.*149G= ENSP00000468145.1:n.*149G=
NM_001060.5:c.*286G= , LRG_578t1:c.*286G= NP_001051.1:n.*286G=
NM_201636.2:c.984-326G= NP_963998.2:n.984-326G=
NM_001060.6:c.*286G= MANE Select NP_001051.1:n.*286G=
NM_201636.3:c.984-326G= NP_963998.2:n.984-326G=