Canonical Allele Identifier: CA403328481
Gene: TBXA2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.3595557A>T (hg19) chr19:g.3595559A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595559A>T , CM000681.2:g.3595559A>T GRCh38
NC_000019.9:g.3595557A>T , CM000681.1:g.3595557A>T GRCh37
NC_000019.8:g.3546557A>T NCBI36
NG_013363.1:g.16275T>A , LRG_578:g.16275T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*129T>A MANE Select ENSP00000364336.4:n.*129T>A
ENST00000375190.8:c.*129T>A ENSP00000364336.3:n.*129T>A
ENST00000411851.3:c.983+178T>A ENSP00000393333.2:n.983+178T>A
ENST00000589966.1:c.772T>A ENSP00000468145.1:p.Leu258Met
NM_001060.5:c.*129T>A , LRG_578t1:c.*129T>A NP_001051.1:n.*129T>A
NM_201636.2:c.983+178T>A NP_963998.2:n.983+178T>A
NM_001060.6:c.*129T>A MANE Select NP_001051.1:n.*129T>A
NM_201636.3:c.983+178T>A NP_963998.2:n.983+178T>A
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