Canonical Allele Identifier: CA403329961

Gene: TBXA2R

Linked Data

• gnomAD v4: 19-3595722-T-C
• MyVariant Identifiers: chr19:g.3595720T>C (hg19) ; chr19:g.3595722T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595722T>C , CM000681.2:g.3595722T>C	GRCh38
NC_000019.9:g.3595720T>C , CM000681.1:g.3595720T>C	GRCh37
NC_000019.8:g.3546720T>C	NCBI36
NG_013363.1:g.16112A>G , LRG_578:g.16112A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.998A>G MANE Select	ENSP00000364336.4:p.Gln333Arg
ENST00000375190.8:c.998A>G	ENSP00000364336.3:p.Gln333Arg
ENST00000411851.3:c.983+15A>G	ENSP00000393333.2:n.983+15A>G
ENST00000589966.1:c.609A>G	ENSP00000468145.1:p.Pro203=
NM_001060.5:c.998A>G , LRG_578t1:c.998A>G	NP_001051.1:p.Gln333Arg
NM_201636.2:c.983+15A>G	NP_963998.2:n.983+15A>G
XM_011528214.1:c.998A>G	XP_011526516.1:p.Gln333Arg
XM_011528214.2:c.998A>G	XP_011526516.1:p.Gln333Arg
NM_001060.6:c.998A>G MANE Select	NP_001051.1:p.Gln333Arg
NM_201636.3:c.983+15A>G	NP_963998.2:n.983+15A>G