Canonical Allele Identifier: CA2318945931
Community Standard Title: NM_001060.6(TBXA2R):c.795C= (p.Ile265=)
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595925G= , CM000681.2:g.3595925G= GRCh38
NC_000019.9:g.3595923G= , CM000681.1:g.3595923G= GRCh37
NC_000019.8:g.3546923G= NCBI36
NG_013363.1:g.15909C= , LRG_578:g.15909C=

Transcript Alleles

HGVS Amino-acid Change
NM_001060.6:c.795C= MANE Select NP_001051.1:p.Ile265=
ENST00000375190.10:c.795C= MANE Select ENSP00000364336.4:p.Ile265=
NM_001060.5:c.795C= , LRG_578t1:c.795C= NP_001051.1:p.Ile265=
NM_201636.2:c.795C= NP_963998.2:p.Ile265=
NM_201636.3:c.795C= NP_963998.2:p.Ile265=
ENST00000375190.8:c.795C= ENSP00000364336.3:p.Ile265=
ENST00000411851.3:c.795C= ENSP00000393333.2:p.Ile265=
ENST00000589966.1:c.406C= ENSP00000468145.1:p.Arg136=
XM_011528214.1:c.795C= XP_011526516.1:p.Ile265=
XM_011528214.2:c.795C= XP_011526516.1:p.Ile265=