Canonical Allele Identifier: CA324115400
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1220422
ClinVar RCV Id: RCV001592680
dbSNP Id: rs73409461
gnomAD v2: 22-38106379-G-T
gnomAD v3: 22-37710372-G-T
gnomAD v4: 22-37710372-G-T
MyVariant Identifiers: chr22:g.38106379G>T (hg19) chr22:g.37710372G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710372G>T , CM000684.2:g.37710372G>T GRCh38
NC_000022.10:g.38106379G>T , CM000684.1:g.38106379G>T GRCh37
NC_000022.9:g.36436325G>T NCBI36
NG_012857.1:g.18385G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.115-55G>T MANE Select ENSP00000496394.1:n.115-55G>T
ENST00000344404.10:c.115-55G>T ENSP00000340312.6:n.115-55G>T
ENST00000406386.7:c.115-55G>T ENSP00000384312.3:n.115-55G>T
ENST00000455236.4:c.1072-55G>T ENSP00000477208.1:n.1072-55G>T
ENST00000492485.5:n.251-55G>T
NM_001039141.2:c.115-55G>T NP_001034230.1:n.115-55G>T
NM_001039141.3:c.115-55G>T MANE Select NP_001034230.1:n.115-55G>T
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