Canonical Allele Identifier: CA514772538
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38130477T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37734470T>C , CM000684.2:g.37734470T>C GRCh38
NC_000022.10:g.38130477T>C , CM000684.1:g.38130477T>C GRCh37
NC_000022.9:g.36460423T>C NCBI36
NG_012857.1:g.42483T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.4134T>C MANE Select ENSP00000496394.1:p.Ser1378=
ENST00000344404.10:c.*3617T>C ENSP00000340312.6:n.*3617T>C
ENST00000406386.7:c.4134T>C ENSP00000384312.3:p.Ser1378=
NM_001039141.2:c.4134T>C NP_001034230.1:p.Ser1378=
XM_011530646.1:c.512-4111A>G XP_011528948.1:n.512-4111A>G
NM_001039141.3:c.4134T>C MANE Select NP_001034230.1:p.Ser1378=
Search 100 bp 5'
Search 100 bp 3'