Canonical Allele Identifier: CA324115243
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs767595487
gnomAD v3: 22-37710222-G-A
gnomAD v4: 22-37710222-G-A
COSMIC: COSN24976973
MyVariant Identifiers: chr22:g.38106229G>A (hg19) chr22:g.37710222G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710222G>A , CM000684.2:g.37710222G>A GRCh38
NC_000022.10:g.38106229G>A , CM000684.1:g.38106229G>A GRCh37
NC_000022.9:g.36436175G>A NCBI36
NG_012857.1:g.18235G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.115-205G>A MANE Select ENSP00000496394.1:n.115-205G>A
ENST00000344404.10:c.115-205G>A ENSP00000340312.6:n.115-205G>A
ENST00000406386.7:c.115-205G>A ENSP00000384312.3:n.115-205G>A
ENST00000455236.4:c.1072-205G>A ENSP00000477208.1:n.1072-205G>A
ENST00000492485.5:n.251-205G>A
NM_001039141.2:c.115-205G>A NP_001034230.1:n.115-205G>A
NM_001039141.3:c.115-205G>A MANE Select NP_001034230.1:n.115-205G>A
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