Canonical Allele Identifier: CA403330264

Gene: TBXA2R

Linked Data

• gnomAD v4: 19-3595756-G-C
• MyVariant Identifiers: chr19:g.3595754G>C (hg19) ; chr19:g.3595756G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595756G>C , CM000681.2:g.3595756G>C	GRCh38
NC_000019.9:g.3595754G>C , CM000681.1:g.3595754G>C	GRCh37
NC_000019.8:g.3546754G>C	NCBI36
NG_013363.1:g.16078C>G , LRG_578:g.16078C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.964C>G MANE Select	ENSP00000364336.4:p.Arg322Gly
ENST00000375190.8:c.964C>G	ENSP00000364336.3:p.Arg322Gly
ENST00000411851.3:c.964C>G	ENSP00000393333.2:p.Arg322Gly
ENST00000589966.1:c.575C>G	ENSP00000468145.1:p.Ser192Trp
NM_001060.5:c.964C>G , LRG_578t1:c.964C>G	NP_001051.1:p.Arg322Gly
NM_201636.2:c.964C>G	NP_963998.2:p.Arg322Gly
XM_011528214.1:c.964C>G	XP_011526516.1:p.Arg322Gly
XM_011528214.2:c.964C>G	XP_011526516.1:p.Arg322Gly
NM_001060.6:c.964C>G MANE Select	NP_001051.1:p.Arg322Gly
NM_201636.3:c.964C>G	NP_963998.2:p.Arg322Gly