Canonical Allele Identifier: CA359724793

Gene: CCNO

Linked Data

• dbSNP Id: rs1403644702
• gnomAD v2: 5-54529122-G-A
• MyVariant Identifiers: chr5:g.54529122G>A (hg19) ; chr5:g.55233294G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233294G>A , CM000667.2:g.55233294G>A	GRCh38
NC_000005.9:g.54529122G>A , CM000667.1:g.54529122G>A	GRCh37
NC_000005.8:g.54564879G>A	NCBI36
NG_034201.1:g.5424C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.230C>T MANE Select	ENSP00000282572.4:p.Ala77Val
ENST00000282572.4:c.230C>T	ENSP00000282572.4:p.Ala77Val
ENST00000501463.2:c.230C>T	ENSP00000422485.1:p.Ala77Val
NM_021147.4:c.230C>T	NP_066970.3:p.Ala77Val
NR_125346.1:n.424C>T
NR_125347.1:n.424C>T
NM_021147.5:c.230C>T MANE Select	NP_066970.3:p.Ala77Val
NR_125346.2:n.315C>T
NR_125347.2:n.315C>T