Canonical Allele Identifier: CA403330819

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1002481239
• gnomAD v4: 19-3595835-G-A
• COSMIC: COSM4077009 ; COSM4077010
• MyVariant Identifiers: chr19:g.3595833G>A (hg19) ; chr19:g.3595835G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595835G>A , CM000681.2:g.3595835G>A	GRCh38
NC_000019.9:g.3595833G>A , CM000681.1:g.3595833G>A	GRCh37
NC_000019.8:g.3546833G>A	NCBI36
NG_013363.1:g.15999C>T , LRG_578:g.15999C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.885C>T MANE Select	ENSP00000364336.4:p.Arg295=
ENST00000375190.8:c.885C>T	ENSP00000364336.3:p.Arg295=
ENST00000411851.3:c.885C>T	ENSP00000393333.2:p.Arg295=
ENST00000589966.1:c.496C>T	ENSP00000468145.1:p.Arg166Cys
NM_001060.5:c.885C>T , LRG_578t1:c.885C>T	NP_001051.1:p.Arg295=
NM_201636.2:c.885C>T	NP_963998.2:p.Arg295=
XM_011528214.1:c.885C>T	XP_011526516.1:p.Arg295=
XM_011528214.2:c.885C>T	XP_011526516.1:p.Arg295=
NM_001060.6:c.885C>T MANE Select	NP_001051.1:p.Arg295=
NM_201636.3:c.885C>T	NP_963998.2:p.Arg295=