Canonical Allele Identifier: CA10224289
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs368773540
ExAC: 22:38129436 G / A
gnomAD v2: 22-38129436-G-A
gnomAD v3: 22-37733429-G-A
gnomAD v4: 22-37733429-G-A
MyVariant Identifiers: chr22:g.38129436G>A (hg19) chr22:g.37733429G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733429G>A , CM000684.2:g.37733429G>A GRCh38
NC_000022.10:g.38129436G>A , CM000684.1:g.38129436G>A GRCh37
NC_000022.9:g.36459382G>A NCBI36
NG_012857.1:g.41442G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4062+17G>A MANE Select ENSP00000496394.1:n.4062+17G>A
ENST00000344404.10:c.*3545+17G>A ENSP00000340312.6:n.*3545+17G>A
ENST00000406386.7:c.4062+17G>A ENSP00000384312.3:n.4062+17G>A
NM_001039141.2:c.4062+17G>A NP_001034230.1:n.4062+17G>A
XM_011530646.1:c.512-3070C>T XP_011528948.1:n.512-3070C>T
NM_001039141.3:c.4062+17G>A MANE Select NP_001034230.1:n.4062+17G>A
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