Canonical Allele Identifier: CA9080763
Gene: TBXA2R HGNC NCBI

Linked Data

ClinVar Variation Id: 2961401
ClinVar RCV Id: RCV003820112 RCV004366750
dbSNP Id: rs780319875
ExAC: 19:3595883 C / T
gnomAD v2: 19-3595883-C-T
gnomAD v3: 19-3595885-C-T
gnomAD v4: 19-3595885-C-T
MyVariant Identifiers: chr19:g.3595883C>T (hg19) chr19:g.3595885C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595885C>T , CM000681.2:g.3595885C>T GRCh38
NC_000019.9:g.3595883C>T , CM000681.1:g.3595883C>T GRCh37
NC_000019.8:g.3546883C>T NCBI36
NG_013363.1:g.15949G>A , LRG_578:g.15949G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.835G>A MANE Select ENSP00000364336.4:p.Ala279Thr
ENST00000375190.8:c.835G>A ENSP00000364336.3:p.Ala279Thr
ENST00000411851.3:c.835G>A ENSP00000393333.2:p.Ala279Thr
ENST00000589966.1:c.446G>A ENSP00000468145.1:p.Arg149His
NM_001060.5:c.835G>A , LRG_578t1:c.835G>A NP_001051.1:p.Ala279Thr
NM_201636.2:c.835G>A NP_963998.2:p.Ala279Thr
XM_011528214.1:c.835G>A XP_011526516.1:p.Ala279Thr
XM_011528214.2:c.835G>A XP_011526516.1:p.Ala279Thr
NM_001060.6:c.835G>A MANE Select NP_001051.1:p.Ala279Thr
NM_201636.3:c.835G>A NP_963998.2:p.Ala279Thr
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