Canonical Allele Identifier: CA411449982
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111802G>T (hg19) chr22:g.37715795G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715795G>T , CM000684.2:g.37715795G>T GRCh38
NC_000022.10:g.38111802G>T , CM000684.1:g.38111802G>T GRCh37
NC_000022.9:g.36441748G>T NCBI36
NG_012857.1:g.23808G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.489G>T MANE Select ENSP00000496394.1:p.Glu163Asp
ENST00000344404.10:c.287G>T ENSP00000340312.6:p.Arg96Met
ENST00000406386.7:c.489G>T ENSP00000384312.3:p.Glu163Asp
ENST00000455236.4:c.1446G>T ENSP00000477208.1:n.1446G>T
ENST00000492485.5:n.423G>T
NM_001039141.2:c.489G>T NP_001034230.1:p.Glu163Asp
NM_001039141.3:c.489G>T MANE Select NP_001034230.1:p.Glu163Asp
Search 100 bp 5'
Search 100 bp 3'