Canonical Allele Identifier: CA118945768

Gene: CCNO

Linked Data

• dbSNP Id: rs1005930703
• gnomAD v2: 5-54529461-A-G
• gnomAD v3: 5-55233633-A-G
• gnomAD v4: 5-55233633-A-G
• MyVariant Identifiers: chr5:g.54529461A>G (hg19) ; chr5:g.55233633A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233633A>G , CM000667.2:g.55233633A>G	GRCh38
NC_000005.9:g.54529461A>G , CM000667.1:g.54529461A>G	GRCh37
NC_000005.8:g.54565218A>G	NCBI36
NG_034201.1:g.5085T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-110T>C	ENSP00000282572.4:n.-110T>C
NM_021147.4:c.-110T>C	NP_066970.3:n.-110T>C
NR_125346.1:n.85T>C
NR_125347.1:n.85T>C