Canonical Allele Identifier: CA2813337191
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595394A>C , CM000681.2:g.3595394A>C GRCh38
NC_000019.9:g.3595392A>C , CM000681.1:g.3595392A>C GRCh37
NC_000019.8:g.3546392A>C NCBI36
NG_013363.1:g.16440T>G , LRG_578:g.16440T>G
NG_031943.1:g.14824A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*294T>G MANE Select ENSP00000364336.4:n.*294T>G
ENST00000375190.8:c.*294T>G ENSP00000364336.3:n.*294T>G
ENST00000411851.3:c.984-318T>G ENSP00000393333.2:n.984-318T>G
ENST00000589966.1:c.*157T>G ENSP00000468145.1:n.*157T>G
NM_001060.5:c.*294T>G , LRG_578t1:c.*294T>G NP_001051.1:n.*294T>G
NM_201636.2:c.984-318T>G NP_963998.2:n.984-318T>G
NM_001060.6:c.*294T>G MANE Select NP_001051.1:n.*294T>G
NM_201636.3:c.984-318T>G NP_963998.2:n.984-318T>G