Canonical Allele Identifier: CA444189611
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1281049463
gnomAD v4: 5-55233583-G-C
MyVariant Identifiers: chr5:g.54529411G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233583G>C , CM000667.2:g.55233583G>C GRCh38
NC_000005.9:g.54529411G>C , CM000667.1:g.54529411G>C GRCh37
NC_000005.8:g.54565168G>C NCBI36
NG_034201.1:g.5135C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-60C>G MANE Select ENSP00000282572.4:n.-60C>G
ENST00000282572.4:c.-60C>G ENSP00000282572.4:n.-60C>G
ENST00000501463.2:c.-60C>G ENSP00000422485.1:n.-60C>G
NM_021147.4:c.-60C>G NP_066970.3:n.-60C>G
NR_125346.1:n.135C>G
NR_125347.1:n.135C>G
NM_021147.5:c.-60C>G MANE Select NP_066970.3:n.-60C>G
NR_125346.2:n.26C>G
NR_125347.2:n.26C>G
Search 100 bp 5'
Search 100 bp 3'