Canonical Allele Identifier: CA10223332
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs755617039
ExAC: 22:38109379 C / T
gnomAD v2: 22-38109379-C-T
gnomAD v4: 22-37713372-C-T
MyVariant Identifiers: chr22:g.38109379C>T (hg19) chr22:g.37713372C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713372C>T , CM000684.2:g.37713372C>T GRCh38
NC_000022.10:g.38109379C>T , CM000684.1:g.38109379C>T GRCh37
NC_000022.9:g.36439325C>T NCBI36
NG_012857.1:g.21385C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.417C>T MANE Select ENSP00000496394.1:p.Asp139=
ENST00000344404.10:c.255-2391C>T ENSP00000340312.6:n.255-2391C>T
ENST00000406386.7:c.417C>T ENSP00000384312.3:p.Asp139=
ENST00000455236.4:c.1374C>T ENSP00000477208.1:n.1374C>T
ENST00000492485.5:n.391-2391C>T
NM_001039141.2:c.417C>T NP_001034230.1:p.Asp139=
NM_001039141.3:c.417C>T MANE Select NP_001034230.1:p.Asp139=
Search 100 bp 5'
Search 100 bp 3'