Canonical Allele Identifier: CA403329093
Gene: TBXA2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.3595584A>C (hg19) chr19:g.3595586A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595586A>C , CM000681.2:g.3595586A>C GRCh38
NC_000019.9:g.3595584A>C , CM000681.1:g.3595584A>C GRCh37
NC_000019.8:g.3546584A>C NCBI36
NG_013363.1:g.16248T>G , LRG_578:g.16248T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*102T>G MANE Select ENSP00000364336.4:n.*102T>G
ENST00000375190.8:c.*102T>G ENSP00000364336.3:n.*102T>G
ENST00000411851.3:c.983+151T>G ENSP00000393333.2:n.983+151T>G
ENST00000589966.1:c.745T>G ENSP00000468145.1:p.Trp249Gly
NM_001060.5:c.*102T>G , LRG_578t1:c.*102T>G NP_001051.1:n.*102T>G
NM_201636.2:c.983+151T>G NP_963998.2:n.983+151T>G
NM_001060.6:c.*102T>G MANE Select NP_001051.1:n.*102T>G
NM_201636.3:c.983+151T>G NP_963998.2:n.983+151T>G
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