Canonical Allele Identifier: CA1547396631
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs919900400
gnomAD v4: 5-55233073-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233073G>A , CM000667.2:g.55233073G>A GRCh38
NC_000005.9:g.54528901G>A , CM000667.1:g.54528901G>A GRCh37
NC_000005.8:g.54564658G>A NCBI36
NG_034201.1:g.5645C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+70C>T MANE Select ENSP00000282572.4:n.381+70C>T
ENST00000282572.4:c.381+70C>T ENSP00000282572.4:n.381+70C>T
ENST00000501463.2:c.*55C>T ENSP00000422485.1:n.*55C>T
NM_021147.4:c.381+70C>T NP_066970.3:n.381+70C>T
NR_125346.1:n.645C>T
NR_125347.1:n.580+65C>T
NM_021147.5:c.381+70C>T MANE Select NP_066970.3:n.381+70C>T
NR_125346.2:n.536C>T
NR_125347.2:n.471+65C>T
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