Canonical Allele Identifier: CA881803564
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1266639196
MyVariant Identifiers: chr19:g.3595415_3595416insGC (hg19) chr19:g.3595417_3595418insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595418_3595419dup , CM000681.2:g.3595418_3595419dup GRCh38
NC_000019.9:g.3595416_3595417dup , CM000681.1:g.3595416_3595417dup GRCh37
NC_000019.8:g.3546416_3546417dup NCBI36
NG_013363.1:g.16415_16416dup , LRG_578:g.16415_16416dup
NG_031943.1:g.14848_14849dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*269_*270dup MANE Select ENSP00000364336.4:n.*269_*270dup
ENST00000375190.8:c.*269_*270dup ENSP00000364336.3:n.*269_*270dup
ENST00000411851.3:c.983+318_983+319dup ENSP00000393333.2:n.983+318_983+319dup
ENST00000589966.1:c.*132_*133dup ENSP00000468145.1:n.*132_*133dup
NM_001060.5:c.*269_*270dup , LRG_578t1:c.*269_*270dup NP_001051.1:n.*269_*270dup
NM_201636.2:c.983+318_983+319dup NP_963998.2:n.983+318_983+319dup
NM_001060.6:c.*269_*270dup MANE Select NP_001051.1:n.*269_*270dup
NM_201636.3:c.983+318_983+319dup NP_963998.2:n.983+318_983+319dup
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