Canonical Allele Identifier: CA2318945771
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595671G= , CM000681.2:g.3595671G= GRCh38
NC_000019.9:g.3595669G= , CM000681.1:g.3595669G= GRCh37
NC_000019.8:g.3546669G= NCBI36
NG_013363.1:g.16163C= , LRG_578:g.16163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*17C= MANE Select ENSP00000364336.4:n.*17C=
ENST00000375190.8:c.*17C= ENSP00000364336.3:n.*17C=
ENST00000411851.3:c.983+66C= ENSP00000393333.2:n.983+66C=
ENST00000589966.1:c.660C= ENSP00000468145.1:p.Ala220=
NM_001060.5:c.*17C= , LRG_578t1:c.*17C= NP_001051.1:n.*17C=
NM_201636.2:c.983+66C= NP_963998.2:n.983+66C=
XM_011528214.1:c.*17C= XP_011526516.1:n.*17C=
XM_011528214.2:c.*17C= XP_011526516.1:n.*17C=
NM_001060.6:c.*17C= MANE Select NP_001051.1:n.*17C=
NM_201636.3:c.983+66C= NP_963998.2:n.983+66C=