Canonical Allele Identifier: CA403331059

Gene: TBXA2R

Linked Data

• dbSNP Id: rs764044824
• gnomAD v2: 19-3595867-C-G
• gnomAD v4: 19-3595869-C-G
• MyVariant Identifiers: chr19:g.3595867C>G (hg19) ; chr19:g.3595869C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595869C>G , CM000681.2:g.3595869C>G	GRCh38
NC_000019.9:g.3595867C>G , CM000681.1:g.3595867C>G	GRCh37
NC_000019.8:g.3546867C>G	NCBI36
NG_013363.1:g.15965G>C , LRG_578:g.15965G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.851G>C MANE Select	ENSP00000364336.4:p.Arg284Pro
ENST00000375190.8:c.851G>C	ENSP00000364336.3:p.Arg284Pro
ENST00000411851.3:c.851G>C	ENSP00000393333.2:p.Arg284Pro
ENST00000589966.1:c.462G>C	ENSP00000468145.1:p.Pro154=
NM_001060.5:c.851G>C , LRG_578t1:c.851G>C	NP_001051.1:p.Arg284Pro
NM_201636.2:c.851G>C	NP_963998.2:p.Arg284Pro
XM_011528214.1:c.851G>C	XP_011526516.1:p.Arg284Pro
XM_011528214.2:c.851G>C	XP_011526516.1:p.Arg284Pro
NM_001060.6:c.851G>C MANE Select	NP_001051.1:p.Arg284Pro
NM_201636.3:c.851G>C	NP_963998.2:p.Arg284Pro