Canonical Allele Identifier: CA403330819
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1002481239
gnomAD v4: 19-3595835-G-A

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=