Canonical Allele Identifier: CA304367741

Gene: TBXA2R

Linked Data

• dbSNP Id: rs5755
• gnomAD v4: 19-3595342-G-A
• MyVariant Identifiers: chr19:g.3595340G>A (hg19) ; chr19:g.3595342G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595342G>A , CM000681.2:g.3595342G>A	GRCh38
NC_000019.9:g.3595340G>A , CM000681.1:g.3595340G>A	GRCh37
NC_000019.8:g.3546340G>A	NCBI36
NG_013363.1:g.16492C>T , LRG_578:g.16492C>T
NG_031943.1:g.14772G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*346C>T MANE Select	ENSP00000364336.4:n.*346C>T
ENST00000375190.8:c.*346C>T	ENSP00000364336.3:n.*346C>T
ENST00000411851.3:c.984-266C>T	ENSP00000393333.2:n.984-266C>T
ENST00000589966.1:c.*209C>T	ENSP00000468145.1:n.*209C>T
NM_001060.5:c.*346C>T , LRG_578t1:c.*346C>T	NP_001051.1:n.*346C>T
NM_201636.2:c.984-266C>T	NP_963998.2:n.984-266C>T
NM_001060.6:c.*346C>T MANE Select	NP_001051.1:n.*346C>T
NM_201636.3:c.984-266C>T	NP_963998.2:n.984-266C>T