Canonical Allele Identifier: CA359726342
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233504-G-T
MyVariant Identifiers: chr5:g.54529332G>T (hg19) chr5:g.55233504G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233504G>T , CM000667.2:g.55233504G>T GRCh38
NC_000005.9:g.54529332G>T , CM000667.1:g.54529332G>T GRCh37
NC_000005.8:g.54565089G>T NCBI36
NG_034201.1:g.5214C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.20C>A MANE Select ENSP00000282572.4:p.Thr7Asn
ENST00000282572.4:c.20C>A ENSP00000282572.4:p.Thr7Asn
ENST00000501463.2:c.20C>A ENSP00000422485.1:p.Thr7Asn
NM_021147.4:c.20C>A NP_066970.3:p.Thr7Asn
NR_125346.1:n.214C>A
NR_125347.1:n.214C>A
NM_021147.5:c.20C>A MANE Select NP_066970.3:p.Thr7Asn
NR_125346.2:n.105C>A
NR_125347.2:n.105C>A
Search 100 bp 5'
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