Canonical Allele Identifier: CA403330801
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs746012285
gnomAD v2: 19-3595830-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595832C>A , CM000681.2:g.3595832C>A GRCh38
NC_000019.9:g.3595830C>A , CM000681.1:g.3595830C>A GRCh37
NC_000019.8:g.3546830C>A NCBI36
NG_013363.1:g.16002G>T , LRG_578:g.16002G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.888G>T MANE Select ENSP00000364336.4:p.Val296=
ENST00000375190.8:c.888G>T ENSP00000364336.3:p.Val296=
ENST00000411851.3:c.888G>T ENSP00000393333.2:p.Val296=
ENST00000589966.1:c.499G>T ENSP00000468145.1:p.Gly167Cys
NM_001060.5:c.888G>T , LRG_578t1:c.888G>T NP_001051.1:p.Val296=
NM_201636.2:c.888G>T NP_963998.2:p.Val296=
XM_011528214.1:c.888G>T XP_011526516.1:p.Val296=
XM_011528214.2:c.888G>T XP_011526516.1:p.Val296=
NM_001060.6:c.888G>T MANE Select NP_001051.1:p.Val296=
NM_201636.3:c.888G>T NP_963998.2:p.Val296=