Canonical Allele Identifier: CA411450602
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs932978968
gnomAD v3: 22-37715899-C-A
gnomAD v4: 22-37715899-C-A
MyVariant Identifiers: chr22:g.38111906C>A (hg19) chr22:g.37715899C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715899C>A , CM000684.2:g.37715899C>A GRCh38
NC_000022.10:g.38111906C>A , CM000684.1:g.38111906C>A GRCh37
NC_000022.9:g.36441852C>A NCBI36
NG_012857.1:g.23912C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.593C>A MANE Select ENSP00000496394.1:p.Pro198His
ENST00000344404.10:c.*76C>A ENSP00000340312.6:n.*76C>A
ENST00000406386.7:c.593C>A ENSP00000384312.3:p.Pro198His
ENST00000455236.4:c.1550C>A ENSP00000477208.1:n.1550C>A
ENST00000492485.5:n.527C>A
NM_001039141.2:c.593C>A NP_001034230.1:p.Pro198His
NM_001039141.3:c.593C>A MANE Select NP_001034230.1:p.Pro198His
Search 100 bp 5'
Search 100 bp 3'