Canonical Allele Identifier: CA403331082
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595873A>C , CM000681.2:g.3595873A>C GRCh38
NC_000019.9:g.3595871A>C , CM000681.1:g.3595871A>C GRCh37
NC_000019.8:g.3546871A>C NCBI36
NG_013363.1:g.15961T>G , LRG_578:g.15961T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.847T>G MANE Select ENSP00000364336.4:p.Ser283Ala
ENST00000375190.8:c.847T>G ENSP00000364336.3:p.Ser283Ala
ENST00000411851.3:c.847T>G ENSP00000393333.2:p.Ser283Ala
ENST00000589966.1:c.458T>G ENSP00000468145.1:p.Val153Gly
NM_001060.5:c.847T>G , LRG_578t1:c.847T>G NP_001051.1:p.Ser283Ala
NM_201636.2:c.847T>G NP_963998.2:p.Ser283Ala
XM_011528214.1:c.847T>G XP_011526516.1:p.Ser283Ala
XM_011528214.2:c.847T>G XP_011526516.1:p.Ser283Ala
NM_001060.6:c.847T>G MANE Select NP_001051.1:p.Ser283Ala
NM_201636.3:c.847T>G NP_963998.2:p.Ser283Ala