Canonical Allele Identifier: CA411449991
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1374574788
gnomAD v2: 22-38111804-C-T
gnomAD v4: 22-37715797-C-T
MyVariant Identifiers: chr22:g.38111804C>T (hg19) chr22:g.37715797C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715797C>T , CM000684.2:g.37715797C>T GRCh38
NC_000022.10:g.38111804C>T , CM000684.1:g.38111804C>T GRCh37
NC_000022.9:g.36441750C>T NCBI36
NG_012857.1:g.23810C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.491C>T MANE Select ENSP00000496394.1:p.Ala164Val
ENST00000344404.10:c.289C>T ENSP00000340312.6:p.Pro97Ser
ENST00000406386.7:c.491C>T ENSP00000384312.3:p.Ala164Val
ENST00000455236.4:c.1448C>T ENSP00000477208.1:n.1448C>T
ENST00000492485.5:n.425C>T
NM_001039141.2:c.491C>T NP_001034230.1:p.Ala164Val
NM_001039141.3:c.491C>T MANE Select NP_001034230.1:p.Ala164Val
Search 100 bp 5'
Search 100 bp 3'