Canonical Allele Identifier: CA133022
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 43849
ClinVar RCV Id: RCV000036816 RCV001560324
dbSNP Id: rs200529550
ExAC: 22:38106521 A / G
gnomAD v2: 22-38106521-A-G
gnomAD v3: 22-37710514-A-G
gnomAD v4: 22-37710514-A-G
MyVariant Identifiers: chr22:g.38106521A>G (hg19) chr22:g.37710514A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710514A>G , CM000684.2:g.37710514A>G GRCh38
NC_000022.10:g.38106521A>G , CM000684.1:g.38106521A>G GRCh37
NC_000022.9:g.36436467A>G NCBI36
NG_012857.1:g.18527A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.202A>G MANE Select ENSP00000496394.1:p.Thr68Ala
ENST00000344404.10:c.202A>G ENSP00000340312.6:p.Thr68Ala
ENST00000406386.7:c.202A>G ENSP00000384312.3:p.Thr68Ala
ENST00000455236.4:c.1159A>G ENSP00000477208.1:n.1159A>G
ENST00000492485.5:n.338A>G
NM_001039141.2:c.202A>G NP_001034230.1:p.Thr68Ala
NM_001039141.3:c.202A>G MANE Select NP_001034230.1:p.Thr68Ala
Search 100 bp 5'
Search 100 bp 3'