Canonical Allele Identifier: CA444397385
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1343291769
gnomAD v2: 5-54529244-G-C
gnomAD v4: 5-55233416-G-C
MyVariant Identifiers: chr5:g.54529244G>C (hg19) chr5:g.55233416G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233416G>C , CM000667.2:g.55233416G>C GRCh38
NC_000005.9:g.54529244G>C , CM000667.1:g.54529244G>C GRCh37
NC_000005.8:g.54565001G>C NCBI36
NG_034201.1:g.5302C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.108C>G MANE Select ENSP00000282572.4:p.Arg36=
ENST00000282572.4:c.108C>G ENSP00000282572.4:p.Arg36=
ENST00000501463.2:c.108C>G ENSP00000422485.1:p.Arg36=
NM_021147.4:c.108C>G NP_066970.3:p.Arg36=
NR_125346.1:n.302C>G
NR_125347.1:n.302C>G
NM_021147.5:c.108C>G MANE Select NP_066970.3:p.Arg36=
NR_125346.2:n.193C>G
NR_125347.2:n.193C>G
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