Canonical Allele Identifier: CA304367925
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs199660119
gnomAD v2: 19-3595866-G-A
gnomAD v3: 19-3595868-G-A
gnomAD v4: 19-3595868-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595868G>A , CM000681.2:g.3595868G>A GRCh38
NC_000019.9:g.3595866G>A , CM000681.1:g.3595866G>A GRCh37
NC_000019.8:g.3546866G>A NCBI36
NG_013363.1:g.15966C>T , LRG_578:g.15966C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.852C>T MANE Select ENSP00000364336.4:p.Arg284=
ENST00000375190.8:c.852C>T ENSP00000364336.3:p.Arg284=
ENST00000411851.3:c.852C>T ENSP00000393333.2:p.Arg284=
ENST00000589966.1:c.463C>T ENSP00000468145.1:p.His155Tyr
NM_001060.5:c.852C>T , LRG_578t1:c.852C>T NP_001051.1:p.Arg284=
NM_201636.2:c.852C>T NP_963998.2:p.Arg284=
XM_011528214.1:c.852C>T XP_011526516.1:p.Arg284=
XM_011528214.2:c.852C>T XP_011526516.1:p.Arg284=
NM_001060.6:c.852C>T MANE Select NP_001051.1:p.Arg284=
NM_201636.3:c.852C>T NP_963998.2:p.Arg284=