Canonical Allele Identifier: CA2656565392
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37713484-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713484A>C , CM000684.2:g.37713484A>C GRCh38
NC_000022.10:g.38109491A>C , CM000684.1:g.38109491A>C GRCh37
NC_000022.9:g.36439437A>C NCBI36
NG_012857.1:g.21497A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.456+73A>C MANE Select ENSP00000496394.1:n.456+73A>C
ENST00000344404.10:c.255-2279A>C ENSP00000340312.6:n.255-2279A>C
ENST00000406386.7:c.456+73A>C ENSP00000384312.3:n.456+73A>C
ENST00000455236.4:c.1413+73A>C ENSP00000477208.1:n.1413+73A>C
ENST00000492485.5:n.391-2279A>C
NM_001039141.2:c.456+73A>C NP_001034230.1:n.456+73A>C
NM_001039141.3:c.456+73A>C MANE Select NP_001034230.1:n.456+73A>C
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