Canonical Allele Identifier: CA324121302
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs932978968
gnomAD v2: 22-38111906-C-T
gnomAD v3: 22-37715899-C-T
gnomAD v4: 22-37715899-C-T
MyVariant Identifiers: chr22:g.38111906C>T (hg19) chr22:g.37715899C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.593C>T MANE Select ENSP00000496394.1:p.Pro198Leu
ENST00000344404.10:c.*76C>T ENSP00000340312.6:n.*76C>T
ENST00000406386.7:c.593C>T ENSP00000384312.3:p.Pro198Leu
ENST00000455236.4:c.1550C>T ENSP00000477208.1:n.1550C>T
ENST00000492485.5:n.527C>T
NM_001039141.2:c.593C>T NP_001034230.1:p.Pro198Leu
NM_001039141.3:c.593C>T MANE Select NP_001034230.1:p.Pro198Leu
Search 100 bp 5'
Search 100 bp 3'