Canonical Allele Identifier: CA411447055
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1275863637

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710527A>G , CM000684.2:g.37710527A>G GRCh38
NC_000022.10:g.38106534A>G , CM000684.1:g.38106534A>G GRCh37
NC_000022.9:g.36436480A>G NCBI36
NG_012857.1:g.18540A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.215A>G MANE Select ENSP00000496394.1:p.Gln72Arg
ENST00000344404.10:c.215A>G ENSP00000340312.6:p.Gln72Arg
ENST00000406386.7:c.215A>G ENSP00000384312.3:p.Gln72Arg
ENST00000455236.4:c.1172A>G ENSP00000477208.1:n.1172A>G
ENST00000492485.5:n.351A>G
NM_001039141.2:c.215A>G NP_001034230.1:p.Gln72Arg
NM_001039141.3:c.215A>G MANE Select NP_001034230.1:p.Gln72Arg