Canonical Allele Identifier: CA359725142
Gene: CCNO HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.54529170A>G (hg19) chr5:g.55233342A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233342A>G , CM000667.2:g.55233342A>G GRCh38
NC_000005.9:g.54529170A>G , CM000667.1:g.54529170A>G GRCh37
NC_000005.8:g.54564927A>G NCBI36
NG_034201.1:g.5376T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.182T>C MANE Select ENSP00000282572.4:p.Phe61Ser
ENST00000282572.4:c.182T>C ENSP00000282572.4:p.Phe61Ser
ENST00000501463.2:c.182T>C ENSP00000422485.1:p.Phe61Ser
NM_021147.4:c.182T>C NP_066970.3:p.Phe61Ser
NR_125346.1:n.376T>C
NR_125347.1:n.376T>C
NM_021147.5:c.182T>C MANE Select NP_066970.3:p.Phe61Ser
NR_125346.2:n.267T>C
NR_125347.2:n.267T>C
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