Canonical Allele Identifier: CA403330980
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595857T>A , CM000681.2:g.3595857T>A GRCh38
NC_000019.9:g.3595855T>A , CM000681.1:g.3595855T>A GRCh37
NC_000019.8:g.3546855T>A NCBI36
NG_013363.1:g.15977A>T , LRG_578:g.15977A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.863A>T MANE Select ENSP00000364336.4:p.Lys288Met
ENST00000375190.8:c.863A>T ENSP00000364336.3:p.Lys288Met
ENST00000411851.3:c.863A>T ENSP00000393333.2:p.Lys288Met
ENST00000589966.1:c.474A>T ENSP00000468145.1:p.Glu158Asp
NM_001060.5:c.863A>T , LRG_578t1:c.863A>T NP_001051.1:p.Lys288Met
NM_201636.2:c.863A>T NP_963998.2:p.Lys288Met
XM_011528214.1:c.863A>T XP_011526516.1:p.Lys288Met
XM_011528214.2:c.863A>T XP_011526516.1:p.Lys288Met
NM_001060.6:c.863A>T MANE Select NP_001051.1:p.Lys288Met
NM_201636.3:c.863A>T NP_963998.2:p.Lys288Met