Canonical Allele Identifier: CA10223371
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 227126
ClinVar RCV Id: RCV000214626 RCV000881690
dbSNP Id: rs116448422
ExAC: 22:38111817 C / A
gnomAD v2: 22-38111817-C-A
gnomAD v3: 22-37715810-C-A
gnomAD v4: 22-37715810-C-A
MyVariant Identifiers: chr22:g.38111817C>A (hg19) chr22:g.37715810C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715810C>A , CM000684.2:g.37715810C>A GRCh38
NC_000022.10:g.38111817C>A , CM000684.1:g.38111817C>A GRCh37
NC_000022.9:g.36441763C>A NCBI36
NG_012857.1:g.23823C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.504C>A MANE Select ENSP00000496394.1:p.Asp168Glu
ENST00000344404.10:c.302C>A ENSP00000340312.6:p.Thr101Lys
ENST00000406386.7:c.504C>A ENSP00000384312.3:p.Asp168Glu
ENST00000455236.4:c.1461C>A ENSP00000477208.1:n.1461C>A
ENST00000492485.5:n.438C>A
NM_001039141.2:c.504C>A NP_001034230.1:p.Asp168Glu
NM_001039141.3:c.504C>A MANE Select NP_001034230.1:p.Asp168Glu
Search 100 bp 5'
Search 100 bp 3'