Canonical Allele Identifier: CA2576567949
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595426T>C , CM000681.2:g.3595426T>C GRCh38
NC_000019.9:g.3595424T>C , CM000681.1:g.3595424T>C GRCh37
NC_000019.8:g.3546424T>C NCBI36
NG_013363.1:g.16408A>G , LRG_578:g.16408A>G
NG_031943.1:g.14856T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*262A>G MANE Select ENSP00000364336.4:n.*262A>G
ENST00000375190.8:c.*262A>G ENSP00000364336.3:n.*262A>G
ENST00000411851.3:c.983+311A>G ENSP00000393333.2:n.983+311A>G
ENST00000589966.1:c.*125A>G ENSP00000468145.1:n.*125A>G
NM_001060.5:c.*262A>G , LRG_578t1:c.*262A>G NP_001051.1:n.*262A>G
NM_201636.2:c.983+311A>G NP_963998.2:n.983+311A>G
NM_001060.6:c.*262A>G MANE Select NP_001051.1:n.*262A>G
NM_201636.3:c.983+311A>G NP_963998.2:n.983+311A>G