Canonical Allele Identifier: CA2318945652
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595443G= , CM000681.2:g.3595443G= GRCh38
NC_000019.9:g.3595441G= , CM000681.1:g.3595441G= GRCh37
NC_000019.8:g.3546441G= NCBI36
NG_013363.1:g.16391C= , LRG_578:g.16391C=
NG_031943.1:g.14873G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*245C= MANE Select ENSP00000364336.4:n.*245C=
ENST00000375190.8:c.*245C= ENSP00000364336.3:n.*245C=
ENST00000411851.3:c.983+294C= ENSP00000393333.2:n.983+294C=
ENST00000589966.1:c.*108C= ENSP00000468145.1:n.*108C=
NM_001060.5:c.*245C= , LRG_578t1:c.*245C= NP_001051.1:n.*245C=
NM_201636.2:c.983+294C= NP_963998.2:n.983+294C=
NM_001060.6:c.*245C= MANE Select NP_001051.1:n.*245C=
NM_201636.3:c.983+294C= NP_963998.2:n.983+294C=