Canonical Allele Identifier: CA411450585
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37715895-T-A
MyVariant Identifiers: chr22:g.38111902T>A (hg19) chr22:g.37715895T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715895T>A , CM000684.2:g.37715895T>A GRCh38
NC_000022.10:g.38111902T>A , CM000684.1:g.38111902T>A GRCh37
NC_000022.9:g.36441848T>A NCBI36
NG_012857.1:g.23908T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.589T>A MANE Select ENSP00000496394.1:p.Ser197Thr
ENST00000344404.10:c.*72T>A ENSP00000340312.6:n.*72T>A
ENST00000406386.7:c.589T>A ENSP00000384312.3:p.Ser197Thr
ENST00000455236.4:c.1546T>A ENSP00000477208.1:n.1546T>A
ENST00000492485.5:n.523T>A
NM_001039141.2:c.589T>A NP_001034230.1:p.Ser197Thr
NM_001039141.3:c.589T>A MANE Select NP_001034230.1:p.Ser197Thr
Search 100 bp 5'
Search 100 bp 3'