Canonical Allele Identifier: CA403330874
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032591795

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595843A>C , CM000681.2:g.3595843A>C GRCh38
NC_000019.9:g.3595841A>C , CM000681.1:g.3595841A>C GRCh37
NC_000019.8:g.3546841A>C NCBI36
NG_013363.1:g.15991T>G , LRG_578:g.15991T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.877T>G MANE Select ENSP00000364336.4:p.Tyr293Asp
ENST00000375190.8:c.877T>G ENSP00000364336.3:p.Tyr293Asp
ENST00000411851.3:c.877T>G ENSP00000393333.2:p.Tyr293Asp
ENST00000589966.1:c.488T>G ENSP00000468145.1:p.Leu163Arg
NM_001060.5:c.877T>G , LRG_578t1:c.877T>G NP_001051.1:p.Tyr293Asp
NM_201636.2:c.877T>G NP_963998.2:p.Tyr293Asp
XM_011528214.1:c.877T>G XP_011526516.1:p.Tyr293Asp
XM_011528214.2:c.877T>G XP_011526516.1:p.Tyr293Asp
NM_001060.6:c.877T>G MANE Select NP_001051.1:p.Tyr293Asp
NM_201636.3:c.877T>G NP_963998.2:p.Tyr293Asp