Canonical Allele Identifier: CA514524929
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38106557A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710550A>C , CM000684.2:g.37710550A>C GRCh38
NC_000022.10:g.38106557A>C , CM000684.1:g.38106557A>C GRCh37
NC_000022.9:g.36436503A>C NCBI36
NG_012857.1:g.18563A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.238A>C MANE Select ENSP00000496394.1:p.Arg80=
ENST00000344404.10:c.238A>C ENSP00000340312.6:p.Arg80=
ENST00000406386.7:c.238A>C ENSP00000384312.3:p.Arg80=
ENST00000455236.4:c.1195A>C ENSP00000477208.1:n.1195A>C
ENST00000492485.5:n.374A>C
NM_001039141.2:c.238A>C NP_001034230.1:p.Arg80=
NM_001039141.3:c.238A>C MANE Select NP_001034230.1:p.Arg80=
Search 100 bp 5'
Search 100 bp 3'