Canonical Allele Identifier: CA559800454
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1345065360
gnomAD v2: 5-54528783-C-G
gnomAD v3: 5-55232955-C-G
gnomAD v4: 5-55232955-C-G
MyVariant Identifiers: chr5:g.54528783C>G (hg19) chr5:g.55232955C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232955C>G , CM000667.2:g.55232955C>G GRCh38
NC_000005.9:g.54528783C>G , CM000667.1:g.54528783C>G GRCh37
NC_000005.8:g.54564540C>G NCBI36
NG_034201.1:g.5763G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+188G>C MANE Select ENSP00000282572.4:n.381+188G>C
ENST00000282572.4:c.381+188G>C ENSP00000282572.4:n.381+188G>C
ENST00000501463.2:c.*173G>C ENSP00000422485.1:n.*173G>C
NM_021147.4:c.381+188G>C NP_066970.3:n.381+188G>C
NR_125346.1:n.763G>C
NR_125347.1:n.580+183G>C
NR_125348.1:n.37G>C
NM_021147.5:c.381+188G>C MANE Select NP_066970.3:n.381+188G>C
NR_125346.2:n.654G>C
NR_125347.2:n.471+183G>C
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