Canonical Allele Identifier: CA2673856340
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232969-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232969C>G , CM000667.2:g.55232969C>G GRCh38
NC_000005.9:g.54528797C>G , CM000667.1:g.54528797C>G GRCh37
NC_000005.8:g.54564554C>G NCBI36
NG_034201.1:g.5749G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+174G>C MANE Select ENSP00000282572.4:n.381+174G>C
ENST00000282572.4:c.381+174G>C ENSP00000282572.4:n.381+174G>C
ENST00000501463.2:c.*159G>C ENSP00000422485.1:n.*159G>C
NM_021147.4:c.381+174G>C NP_066970.3:n.381+174G>C
NR_125346.1:n.749G>C
NR_125347.1:n.580+169G>C
NR_125348.1:n.23G>C
NM_021147.5:c.381+174G>C MANE Select NP_066970.3:n.381+174G>C
NR_125346.2:n.640G>C
NR_125347.2:n.471+169G>C
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