Canonical Allele Identifier: CA2584493665
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595399-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595399A>G , CM000681.2:g.3595399A>G GRCh38
NC_000019.9:g.3595397A>G , CM000681.1:g.3595397A>G GRCh37
NC_000019.8:g.3546397A>G NCBI36
NG_013363.1:g.16435T>C , LRG_578:g.16435T>C
NG_031943.1:g.14829A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*289T>C MANE Select ENSP00000364336.4:n.*289T>C
ENST00000375190.8:c.*289T>C ENSP00000364336.3:n.*289T>C
ENST00000411851.3:c.984-323T>C ENSP00000393333.2:n.984-323T>C
ENST00000589966.1:c.*152T>C ENSP00000468145.1:n.*152T>C
NM_001060.5:c.*289T>C , LRG_578t1:c.*289T>C NP_001051.1:n.*289T>C
NM_201636.2:c.984-323T>C NP_963998.2:n.984-323T>C
NM_001060.6:c.*289T>C MANE Select NP_001051.1:n.*289T>C
NM_201636.3:c.984-323T>C NP_963998.2:n.984-323T>C