Canonical Allele Identifier: CA411450592
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111903C>G (hg19) chr22:g.37715896C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715896C>G , CM000684.2:g.37715896C>G GRCh38
NC_000022.10:g.38111903C>G , CM000684.1:g.38111903C>G GRCh37
NC_000022.9:g.36441849C>G NCBI36
NG_012857.1:g.23909C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.590C>G MANE Select ENSP00000496394.1:p.Ser197Cys
ENST00000344404.10:c.*73C>G ENSP00000340312.6:n.*73C>G
ENST00000406386.7:c.590C>G ENSP00000384312.3:p.Ser197Cys
ENST00000455236.4:c.1547C>G ENSP00000477208.1:n.1547C>G
ENST00000492485.5:n.524C>G
NM_001039141.2:c.590C>G NP_001034230.1:p.Ser197Cys
NM_001039141.3:c.590C>G MANE Select NP_001034230.1:p.Ser197Cys
Search 100 bp 5'
Search 100 bp 3'