Canonical Allele Identifier: CA639202102
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1436092618
gnomAD v2: 22-38164045-T-A
gnomAD v4: 22-37768038-T-A
MyVariant Identifiers: chr22:g.38164045T>A (hg19) chr22:g.37768038T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768038T>A , CM000684.2:g.37768038T>A GRCh38
NC_000022.10:g.38164045T>A , CM000684.1:g.38164045T>A GRCh37
NC_000022.9:g.36493991T>A NCBI36
NG_012857.1:g.76051T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6473-36T>A MANE Select ENSP00000496394.1:n.6473-36T>A
ENST00000344404.10:c.*5956-36T>A ENSP00000340312.6:n.*5956-36T>A
ENST00000403663.6:c.1334-36T>A ENSP00000386026.2:n.1334-36T>A
ENST00000406386.7:c.6473-36T>A ENSP00000384312.3:n.6473-36T>A
NM_001039141.2:c.6473-36T>A NP_001034230.1:n.6473-36T>A
NM_007032.5:c.1334-36T>A NP_008963.3:n.1334-36T>A
NM_001039141.3:c.6473-36T>A MANE Select NP_001034230.1:n.6473-36T>A
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