Canonical Allele Identifier: CA812219041
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1486625589
MyVariant Identifiers: chr5:g.54529371T>G (hg19) chr5:g.55233543T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233543T>G , CM000667.2:g.55233543T>G GRCh38
NC_000005.9:g.54529371T>G , CM000667.1:g.54529371T>G GRCh37
NC_000005.8:g.54565128T>G NCBI36
NG_034201.1:g.5175A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-20A>C MANE Select ENSP00000282572.4:n.-20A>C
ENST00000282572.4:c.-20A>C ENSP00000282572.4:n.-20A>C
ENST00000501463.2:c.-20A>C ENSP00000422485.1:n.-20A>C
NM_021147.4:c.-20A>C NP_066970.3:n.-20A>C
NR_125346.1:n.175A>C
NR_125347.1:n.175A>C
NM_021147.5:c.-20A>C MANE Select NP_066970.3:n.-20A>C
NR_125346.2:n.66A>C
NR_125347.2:n.66A>C
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