Canonical Allele Identifier: CA118944661

Gene: CCNO

Linked Data

• dbSNP Id: rs376062835
• gnomAD v3: 5-55232950-G-C
• gnomAD v4: 5-55232950-G-C
• MyVariant Identifiers: chr5:g.54528778G>C (hg19) ; chr5:g.55232950G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232950G>C , CM000667.2:g.55232950G>C	GRCh38
NC_000005.9:g.54528778G>C , CM000667.1:g.54528778G>C	GRCh37
NC_000005.8:g.54564535G>C	NCBI36
NG_034201.1:g.5768C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+193C>G MANE Select	ENSP00000282572.4:n.381+193C>G
ENST00000282572.4:c.381+193C>G	ENSP00000282572.4:n.381+193C>G
ENST00000501463.2:c.*178C>G	ENSP00000422485.1:n.*178C>G
NM_021147.4:c.381+193C>G	NP_066970.3:n.381+193C>G
NR_125346.1:n.768C>G
NR_125347.1:n.580+188C>G
NR_125348.1:n.42C>G
NM_021147.5:c.381+193C>G MANE Select	NP_066970.3:n.381+193C>G
NR_125346.2:n.659C>G
NR_125347.2:n.471+188C>G