Canonical Allele Identifier: CA411450022
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111809A>G (hg19) chr22:g.37715802A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715802A>G , CM000684.2:g.37715802A>G GRCh38
NC_000022.10:g.38111809A>G , CM000684.1:g.38111809A>G GRCh37
NC_000022.9:g.36441755A>G NCBI36
NG_012857.1:g.23815A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.496A>G MANE Select ENSP00000496394.1:p.Ser166Gly
ENST00000344404.10:c.294A>G ENSP00000340312.6:p.Pro98=
ENST00000406386.7:c.496A>G ENSP00000384312.3:p.Ser166Gly
ENST00000455236.4:c.1453A>G ENSP00000477208.1:n.1453A>G
ENST00000492485.5:n.430A>G
NM_001039141.2:c.496A>G NP_001034230.1:p.Ser166Gly
NM_001039141.3:c.496A>G MANE Select NP_001034230.1:p.Ser166Gly
Search 100 bp 5'
Search 100 bp 3'