Canonical Allele Identifier: CA514772094
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v3: 22-37725766-C-A
gnomAD v4: 22-37725766-C-A
MyVariant Identifiers: chr22:g.38121773C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37725766C>A , CM000684.2:g.37725766C>A GRCh38
NC_000022.10:g.38121773C>A , CM000684.1:g.38121773C>A GRCh37
NC_000022.9:g.36451719C>A NCBI36
NG_012857.1:g.33779C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.3210C>A MANE Select ENSP00000496394.1:p.Ala1070=
ENST00000344404.10:c.*2693C>A ENSP00000340312.6:n.*2693C>A
ENST00000406386.7:c.3210C>A ENSP00000384312.3:p.Ala1070=
ENST00000455236.4:c.4167C>A ENSP00000477208.1:n.4167C>A
ENST00000492485.5:n.3144C>A
NM_001039141.2:c.3210C>A NP_001034230.1:p.Ala1070=
NM_001039141.3:c.3210C>A MANE Select NP_001034230.1:p.Ala1070=
Search 100 bp 5'
Search 100 bp 3'