Canonical Allele Identifier: CA2584493702
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595449-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595449G>A , CM000681.2:g.3595449G>A GRCh38
NC_000019.9:g.3595447G>A , CM000681.1:g.3595447G>A GRCh37
NC_000019.8:g.3546447G>A NCBI36
NG_013363.1:g.16385C>T , LRG_578:g.16385C>T
NG_031943.1:g.14879G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*239C>T MANE Select ENSP00000364336.4:n.*239C>T
ENST00000375190.8:c.*239C>T ENSP00000364336.3:n.*239C>T
ENST00000411851.3:c.983+288C>T ENSP00000393333.2:n.983+288C>T
ENST00000589966.1:c.*102C>T ENSP00000468145.1:n.*102C>T
NM_001060.5:c.*239C>T , LRG_578t1:c.*239C>T NP_001051.1:n.*239C>T
NM_201636.2:c.983+288C>T NP_963998.2:n.983+288C>T
NM_001060.6:c.*239C>T MANE Select NP_001051.1:n.*239C>T
NM_201636.3:c.983+288C>T NP_963998.2:n.983+288C>T