Canonical Allele Identifier: CA118945775
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs768942525
gnomAD v3: 5-55233634-A-G
gnomAD v4: 5-55233634-A-G
MyVariant Identifiers: chr5:g.54529462A>G (hg19) chr5:g.55233634A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233634A>G , CM000667.2:g.55233634A>G GRCh38
NC_000005.9:g.54529462A>G , CM000667.1:g.54529462A>G GRCh37
NC_000005.8:g.54565219A>G NCBI36
NG_034201.1:g.5084T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-111T>C ENSP00000282572.4:n.-111T>C
NM_021147.4:c.-111T>C NP_066970.3:n.-111T>C
NR_125346.1:n.84T>C
NR_125347.1:n.84T>C
Search 100 bp 5'
Search 100 bp 3'