Canonical Allele Identifier: CA2584493810
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595665-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595665G>T , CM000681.2:g.3595665G>T GRCh38
NC_000019.9:g.3595663G>T , CM000681.1:g.3595663G>T GRCh37
NC_000019.8:g.3546663G>T NCBI36
NG_013363.1:g.16169C>A , LRG_578:g.16169C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*23C>A MANE Select ENSP00000364336.4:n.*23C>A
ENST00000375190.8:c.*23C>A ENSP00000364336.3:n.*23C>A
ENST00000411851.3:c.983+72C>A ENSP00000393333.2:n.983+72C>A
ENST00000589966.1:c.666C>A ENSP00000468145.1:p.Pro222=
NM_001060.5:c.*23C>A , LRG_578t1:c.*23C>A NP_001051.1:n.*23C>A
NM_201636.2:c.983+72C>A NP_963998.2:n.983+72C>A
XM_011528214.1:c.*23C>A XP_011526516.1:n.*23C>A
XM_011528214.2:c.*23C>A XP_011526516.1:n.*23C>A
NM_001060.6:c.*23C>A MANE Select NP_001051.1:n.*23C>A
NM_201636.3:c.983+72C>A NP_963998.2:n.983+72C>A