Canonical Allele Identifier: CA514528358
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37768120-G-A
MyVariant Identifiers: chr22:g.38164127G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768120G>A , CM000684.2:g.37768120G>A GRCh38
NC_000022.10:g.38164127G>A , CM000684.1:g.38164127G>A GRCh37
NC_000022.9:g.36494073G>A NCBI36
NG_012857.1:g.76133G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6519G>A MANE Select ENSP00000496394.1:p.Glu2173=
ENST00000344404.10:c.*6002G>A ENSP00000340312.6:n.*6002G>A
ENST00000403663.6:c.1380G>A ENSP00000386026.2:p.Glu460=
ENST00000406386.7:c.6519G>A ENSP00000384312.3:p.Glu2173=
NM_001039141.2:c.6519G>A NP_001034230.1:p.Glu2173=
NM_007032.5:c.1380G>A NP_008963.3:p.Glu460=
NM_001039141.3:c.6519G>A MANE Select NP_001034230.1:p.Glu2173=
Search 100 bp 5'
Search 100 bp 3'