Canonical Allele Identifier: CA10223437
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1050176
ClinVar RCV Id: RCV001357186 RCV002476636 RCV003946021
dbSNP Id: rs144995033
ExAC: 22:38119272 C / T
gnomAD v2: 22-38119272-C-T
gnomAD v3: 22-37723265-C-T
gnomAD v4: 22-37723265-C-T
COSMIC: COSM267881
MyVariant Identifiers: chr22:g.38119272C>T (hg19) chr22:g.37723265C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37723265C>T , CM000684.2:g.37723265C>T GRCh38
NC_000022.10:g.38119272C>T , CM000684.1:g.38119272C>T GRCh37
NC_000022.9:g.36449218C>T NCBI36
NG_012857.1:g.31278C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.709C>T MANE Select ENSP00000496394.1:p.Arg237Trp
ENST00000344404.10:c.*192C>T ENSP00000340312.6:n.*192C>T
ENST00000406386.7:c.709C>T ENSP00000384312.3:p.Arg237Trp
ENST00000455236.4:c.1666C>T ENSP00000477208.1:n.1666C>T
ENST00000492485.5:n.643C>T
NM_001039141.2:c.709C>T NP_001034230.1:p.Arg237Trp
NM_001039141.3:c.709C>T MANE Select NP_001034230.1:p.Arg237Trp
Search 100 bp 5'
Search 100 bp 3'