Canonical Allele Identifier: CA403331023

Gene: TBXA2R

Linked Data

• dbSNP Id: rs61731124
• gnomAD v3: 19-3595863-G-C
• gnomAD v4: 19-3595863-G-C
• MyVariant Identifiers: chr19:g.3595861G>C (hg19) ; chr19:g.3595863G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595863G>C , CM000681.2:g.3595863G>C	GRCh38
NC_000019.9:g.3595861G>C , CM000681.1:g.3595861G>C	GRCh37
NC_000019.8:g.3546861G>C	NCBI36
NG_013363.1:g.15971C>G , LRG_578:g.15971C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.857C>G MANE Select	ENSP00000364336.4:p.Thr286Arg
ENST00000375190.8:c.857C>G	ENSP00000364336.3:p.Thr286Arg
ENST00000411851.3:c.857C>G	ENSP00000393333.2:p.Thr286Arg
ENST00000589966.1:c.468C>G	ENSP00000468145.1:p.His156Gln
NM_001060.5:c.857C>G , LRG_578t1:c.857C>G	NP_001051.1:p.Thr286Arg
NM_201636.2:c.857C>G	NP_963998.2:p.Thr286Arg
XM_011528214.1:c.857C>G	XP_011526516.1:p.Thr286Arg
XM_011528214.2:c.857C>G	XP_011526516.1:p.Thr286Arg
NM_001060.6:c.857C>G MANE Select	NP_001051.1:p.Thr286Arg
NM_201636.3:c.857C>G	NP_963998.2:p.Thr286Arg