Canonical Allele Identifier: CA359724987
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1359543148
gnomAD v2: 5-54529147-C-T
gnomAD v4: 5-55233319-C-T
MyVariant Identifiers: chr5:g.54529147C>T (hg19) chr5:g.55233319C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233319C>T , CM000667.2:g.55233319C>T GRCh38
NC_000005.9:g.54529147C>T , CM000667.1:g.54529147C>T GRCh37
NC_000005.8:g.54564904C>T NCBI36
NG_034201.1:g.5399G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.205G>A MANE Select ENSP00000282572.4:p.Asp69Asn
ENST00000282572.4:c.205G>A ENSP00000282572.4:p.Asp69Asn
ENST00000501463.2:c.205G>A ENSP00000422485.1:p.Asp69Asn
NM_021147.4:c.205G>A NP_066970.3:p.Asp69Asn
NR_125346.1:n.399G>A
NR_125347.1:n.399G>A
NM_021147.5:c.205G>A MANE Select NP_066970.3:p.Asp69Asn
NR_125346.2:n.290G>A
NR_125347.2:n.290G>A
Search 100 bp 5'
Search 100 bp 3'