Canonical Allele Identifier: CA1025581896
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1156846147

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713167C>G , CM000684.2:g.37713167C>G GRCh38
NC_000022.10:g.38109174C>G , CM000684.1:g.38109174C>G GRCh37
NC_000022.9:g.36439120C>G NCBI36
NG_012857.1:g.21180C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.255-43C>G MANE Select ENSP00000496394.1:n.255-43C>G
ENST00000344404.10:c.255-2596C>G ENSP00000340312.6:n.255-2596C>G
ENST00000406386.7:c.255-43C>G ENSP00000384312.3:n.255-43C>G
ENST00000455236.4:c.1212-43C>G ENSP00000477208.1:n.1212-43C>G
ENST00000492485.5:n.391-2596C>G
NM_001039141.2:c.255-43C>G NP_001034230.1:n.255-43C>G
NM_001039141.3:c.255-43C>G MANE Select NP_001034230.1:n.255-43C>G