Canonical Allele Identifier: CA411449938
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111797G>T (hg19) chr22:g.37715790G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715790G>T , CM000684.2:g.37715790G>T GRCh38
NC_000022.10:g.38111797G>T , CM000684.1:g.38111797G>T GRCh37
NC_000022.9:g.36441743G>T NCBI36
NG_012857.1:g.23803G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.484G>T MANE Select ENSP00000496394.1:p.Glu162Ter
ENST00000344404.10:c.282G>T ENSP00000340312.6:p.Arg94Ser
ENST00000406386.7:c.484G>T ENSP00000384312.3:p.Glu162Ter
ENST00000455236.4:c.1441G>T ENSP00000477208.1:n.1441G>T
ENST00000492485.5:n.418G>T
NM_001039141.2:c.484G>T NP_001034230.1:p.Glu162Ter
NM_001039141.3:c.484G>T MANE Select NP_001034230.1:p.Glu162Ter
Search 100 bp 5'
Search 100 bp 3'