Canonical Allele Identifier: CA324115929
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1046976984
gnomAD v3: 22-37710814-T-A
gnomAD v4: 22-37710814-T-A
MyVariant Identifiers: chr22:g.38106821T>A (hg19) chr22:g.37710814T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710814T>A , CM000684.2:g.37710814T>A GRCh38
NC_000022.10:g.38106821T>A , CM000684.1:g.38106821T>A GRCh37
NC_000022.9:g.36436767T>A NCBI36
NG_012857.1:g.18827T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254+248T>A MANE Select ENSP00000496394.1:n.254+248T>A
ENST00000344404.10:c.254+248T>A ENSP00000340312.6:n.254+248T>A
ENST00000406386.7:c.254+248T>A ENSP00000384312.3:n.254+248T>A
ENST00000455236.4:c.1211+248T>A ENSP00000477208.1:n.1211+248T>A
ENST00000492485.5:n.390+248T>A
NM_001039141.2:c.254+248T>A NP_001034230.1:n.254+248T>A
NM_001039141.3:c.254+248T>A MANE Select NP_001034230.1:n.254+248T>A
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