Canonical Allele Identifier: CA559800455

Gene: CCNO

Linked Data

• dbSNP Id: rs957049637
• gnomAD v2: 5-54528801-C-G
• gnomAD v3: 5-55232973-C-G
• gnomAD v4: 5-55232973-C-G
• MyVariant Identifiers: chr5:g.54528801C>G (hg19) ; chr5:g.55232973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232973C>G , CM000667.2:g.55232973C>G	GRCh38
NC_000005.9:g.54528801C>G , CM000667.1:g.54528801C>G	GRCh37
NC_000005.8:g.54564558C>G	NCBI36
NG_034201.1:g.5745G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+170G>C MANE Select	ENSP00000282572.4:n.381+170G>C
ENST00000282572.4:c.381+170G>C	ENSP00000282572.4:n.381+170G>C
ENST00000501463.2:c.*155G>C	ENSP00000422485.1:n.*155G>C
NM_021147.4:c.381+170G>C	NP_066970.3:n.381+170G>C
NR_125346.1:n.745G>C
NR_125347.1:n.580+165G>C
NR_125348.1:n.19G>C
NM_021147.5:c.381+170G>C MANE Select	NP_066970.3:n.381+170G>C
NR_125346.2:n.636G>C
NR_125347.2:n.471+165G>C