Canonical Allele Identifier: CA411447086
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1274489958
gnomAD v2: 22-38106548-C-A
gnomAD v4: 22-37710541-C-A
MyVariant Identifiers: chr22:g.38106548C>A (hg19) chr22:g.37710541C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710541C>A , CM000684.2:g.37710541C>A GRCh38
NC_000022.10:g.38106548C>A , CM000684.1:g.38106548C>A GRCh37
NC_000022.9:g.36436494C>A NCBI36
NG_012857.1:g.18554C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.229C>A MANE Select ENSP00000496394.1:p.Pro77Thr
ENST00000344404.10:c.229C>A ENSP00000340312.6:p.Pro77Thr
ENST00000406386.7:c.229C>A ENSP00000384312.3:p.Pro77Thr
ENST00000455236.4:c.1186C>A ENSP00000477208.1:n.1186C>A
ENST00000492485.5:n.365C>A
NM_001039141.2:c.229C>A NP_001034230.1:p.Pro77Thr
NM_001039141.3:c.229C>A MANE Select NP_001034230.1:p.Pro77Thr
Search 100 bp 5'
Search 100 bp 3'