Canonical Allele Identifier: CA10224299
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1177696
ClinVar RCV Id: RCV001533818
dbSNP Id: rs73883905
ExAC: 22:38130375 A / C
gnomAD v2: 22-38130375-A-C
gnomAD v3: 22-37734368-A-C
gnomAD v4: 22-37734368-A-C
MyVariant Identifiers: chr22:g.38130375A>C (hg19) chr22:g.37734368A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37734368A>C , CM000684.2:g.37734368A>C GRCh38
NC_000022.10:g.38130375A>C , CM000684.1:g.38130375A>C GRCh37
NC_000022.9:g.36460321A>C NCBI36
NG_012857.1:g.42381A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.4063-31A>C MANE Select ENSP00000496394.1:n.4063-31A>C
ENST00000344404.10:c.*3546-31A>C ENSP00000340312.6:n.*3546-31A>C
ENST00000406386.7:c.4063-31A>C ENSP00000384312.3:n.4063-31A>C
NM_001039141.2:c.4063-31A>C NP_001034230.1:n.4063-31A>C
XM_011530646.1:c.512-4009T>G XP_011528948.1:n.512-4009T>G
NM_001039141.3:c.4063-31A>C MANE Select NP_001034230.1:n.4063-31A>C
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