Canonical Allele Identifier: CA411448249
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs200112121
gnomAD v3: 22-37713336-C-A
gnomAD v4: 22-37713336-C-A
MyVariant Identifiers: chr22:g.38109343C>A (hg19) chr22:g.37713336C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713336C>A , CM000684.2:g.37713336C>A GRCh38
NC_000022.10:g.38109343C>A , CM000684.1:g.38109343C>A GRCh37
NC_000022.9:g.36439289C>A NCBI36
NG_012857.1:g.21349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.381C>A MANE Select ENSP00000496394.1:p.Asn127Lys
ENST00000344404.10:c.255-2427C>A ENSP00000340312.6:n.255-2427C>A
ENST00000406386.7:c.381C>A ENSP00000384312.3:p.Asn127Lys
ENST00000455236.4:c.1338C>A ENSP00000477208.1:n.1338C>A
ENST00000492485.5:n.391-2427C>A
NM_001039141.2:c.381C>A NP_001034230.1:p.Asn127Lys
NM_001039141.3:c.381C>A MANE Select NP_001034230.1:p.Asn127Lys
Search 100 bp 5'
Search 100 bp 3'