Canonical Allele Identifier: CA514525804
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38129326C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733319C>G , CM000684.2:g.37733319C>G GRCh38
NC_000022.10:g.38129326C>G , CM000684.1:g.38129326C>G GRCh37
NC_000022.9:g.36459272C>G NCBI36
NG_012857.1:g.41332C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3969C>G MANE Select ENSP00000496394.1:p.Ala1323=
ENST00000344404.10:c.*3452C>G ENSP00000340312.6:n.*3452C>G
ENST00000406386.7:c.3969C>G ENSP00000384312.3:p.Ala1323=
NM_001039141.2:c.3969C>G NP_001034230.1:p.Ala1323=
XM_011530646.1:c.512-2960G>C XP_011528948.1:n.512-2960G>C
NM_001039141.3:c.3969C>G MANE Select NP_001034230.1:p.Ala1323=
Search 100 bp 5'
Search 100 bp 3'