Canonical Allele Identifier: CA10223392
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1223794
ClinVar RCV Id: RCV001596588
dbSNP Id: rs200786015
ExAC: 22:38111900 G / C
gnomAD v2: 22-38111900-G-C
gnomAD v3: 22-37715893-G-C
gnomAD v4: 22-37715893-G-C
MyVariant Identifiers: chr22:g.38111900G>C (hg19) chr22:g.37715893G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715893G>C , CM000684.2:g.37715893G>C GRCh38
NC_000022.10:g.38111900G>C , CM000684.1:g.38111900G>C GRCh37
NC_000022.9:g.36441846G>C NCBI36
NG_012857.1:g.23906G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.587G>C MANE Select ENSP00000496394.1:p.Arg196Thr
ENST00000344404.10:c.*70G>C ENSP00000340312.6:n.*70G>C
ENST00000406386.7:c.587G>C ENSP00000384312.3:p.Arg196Thr
ENST00000455236.4:c.1544G>C ENSP00000477208.1:n.1544G>C
ENST00000492485.5:n.521G>C
NM_001039141.2:c.587G>C NP_001034230.1:p.Arg196Thr
NM_001039141.3:c.587G>C MANE Select NP_001034230.1:p.Arg196Thr
Search 100 bp 5'
Search 100 bp 3'