Canonical Allele Identifier: CA411487423
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38129385T>A (hg19) chr22:g.37733378T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733378T>A , CM000684.2:g.37733378T>A GRCh38
NC_000022.10:g.38129385T>A , CM000684.1:g.38129385T>A GRCh37
NC_000022.9:g.36459331T>A NCBI36
NG_012857.1:g.41391T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4028T>A MANE Select ENSP00000496394.1:p.Leu1343His
ENST00000344404.10:c.*3511T>A ENSP00000340312.6:n.*3511T>A
ENST00000406386.7:c.4028T>A ENSP00000384312.3:p.Leu1343His
NM_001039141.2:c.4028T>A NP_001034230.1:p.Leu1343His
XM_011530646.1:c.512-3019A>T XP_011528948.1:n.512-3019A>T
NM_001039141.3:c.4028T>A MANE Select NP_001034230.1:p.Leu1343His
Search 100 bp 5'
Search 100 bp 3'