Canonical Allele Identifier: CA403331251
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595908C>A , CM000681.2:g.3595908C>A GRCh38
NC_000019.9:g.3595906C>A , CM000681.1:g.3595906C>A GRCh37
NC_000019.8:g.3546906C>A NCBI36
NG_013363.1:g.15926G>T , LRG_578:g.15926G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.812G>T MANE Select ENSP00000364336.4:p.Arg271Leu
ENST00000375190.8:c.812G>T ENSP00000364336.3:p.Arg271Leu
ENST00000411851.3:c.812G>T ENSP00000393333.2:p.Arg271Leu
ENST00000589966.1:c.423G>T ENSP00000468145.1:p.Ala141=
NM_001060.5:c.812G>T , LRG_578t1:c.812G>T NP_001051.1:p.Arg271Leu
NM_201636.2:c.812G>T NP_963998.2:p.Arg271Leu
XM_011528214.1:c.812G>T XP_011526516.1:p.Arg271Leu
XM_011528214.2:c.812G>T XP_011526516.1:p.Arg271Leu
NM_001060.6:c.812G>T MANE Select NP_001051.1:p.Arg271Leu
NM_201636.3:c.812G>T NP_963998.2:p.Arg271Leu