Canonical Allele Identifier: CA514772081
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38121767A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37725760A>C , CM000684.2:g.37725760A>C GRCh38
NC_000022.10:g.38121767A>C , CM000684.1:g.38121767A>C GRCh37
NC_000022.9:g.36451713A>C NCBI36
NG_012857.1:g.33773A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.3204A>C MANE Select ENSP00000496394.1:p.Arg1068=
ENST00000344404.10:c.*2687A>C ENSP00000340312.6:n.*2687A>C
ENST00000406386.7:c.3204A>C ENSP00000384312.3:p.Arg1068=
ENST00000455236.4:c.4161A>C ENSP00000477208.1:n.4161A>C
ENST00000492485.5:n.3138A>C
NM_001039141.2:c.3204A>C NP_001034230.1:p.Arg1068=
NM_001039141.3:c.3204A>C MANE Select NP_001034230.1:p.Arg1068=
Search 100 bp 5'
Search 100 bp 3'