Canonical Allele Identifier: CA403329085
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595584-C-T
MyVariant Identifiers: chr19:g.3595582C>T (hg19) chr19:g.3595584C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595584C>T , CM000681.2:g.3595584C>T GRCh38
NC_000019.9:g.3595582C>T , CM000681.1:g.3595582C>T GRCh37
NC_000019.8:g.3546582C>T NCBI36
NG_013363.1:g.16250G>A , LRG_578:g.16250G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*104G>A MANE Select ENSP00000364336.4:n.*104G>A
ENST00000375190.8:c.*104G>A ENSP00000364336.3:n.*104G>A
ENST00000411851.3:c.983+153G>A ENSP00000393333.2:n.983+153G>A
ENST00000589966.1:c.747G>A ENSP00000468145.1:p.Trp249Ter
NM_001060.5:c.*104G>A , LRG_578t1:c.*104G>A NP_001051.1:n.*104G>A
NM_201636.2:c.983+153G>A NP_963998.2:n.983+153G>A
NM_001060.6:c.*104G>A MANE Select NP_001051.1:n.*104G>A
NM_201636.3:c.983+153G>A NP_963998.2:n.983+153G>A
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