Canonical Allele Identifier: CA411449934
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1392181685
gnomAD v4: 22-37715790-G-A
MyVariant Identifiers: chr22:g.38111797G>A (hg19) chr22:g.37715790G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.484G>A MANE Select ENSP00000496394.1:p.Glu162Lys
ENST00000344404.10:c.282G>A ENSP00000340312.6:p.Arg94=
ENST00000406386.7:c.484G>A ENSP00000384312.3:p.Glu162Lys
ENST00000455236.4:c.1441G>A ENSP00000477208.1:n.1441G>A
ENST00000492485.5:n.418G>A
NM_001039141.2:c.484G>A NP_001034230.1:p.Glu162Lys
NM_001039141.3:c.484G>A MANE Select NP_001034230.1:p.Glu162Lys
Search 100 bp 5'
Search 100 bp 3'