Canonical Allele Identifier: CA411448726
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2428977
ClinVar RCV Id: RCV003123218
gnomAD v4: 22-37713388-G-A
MyVariant Identifiers: chr22:g.38109395G>A (hg19) chr22:g.37713388G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713388G>A , CM000684.2:g.37713388G>A GRCh38
NC_000022.10:g.38109395G>A , CM000684.1:g.38109395G>A GRCh37
NC_000022.9:g.36439341G>A NCBI36
NG_012857.1:g.21401G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.433G>A MANE Select ENSP00000496394.1:p.Asp145Asn
ENST00000344404.10:c.255-2375G>A ENSP00000340312.6:n.255-2375G>A
ENST00000406386.7:c.433G>A ENSP00000384312.3:p.Asp145Asn
ENST00000455236.4:c.1390G>A ENSP00000477208.1:n.1390G>A
ENST00000492485.5:n.391-2375G>A
NM_001039141.2:c.433G>A NP_001034230.1:p.Asp145Asn
NM_001039141.3:c.433G>A MANE Select NP_001034230.1:p.Asp145Asn
Search 100 bp 5'
Search 100 bp 3'