Canonical Allele Identifier: CA444396944
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1366870730
gnomAD v2: 5-54529091-G-C
gnomAD v3: 5-55233263-G-C
gnomAD v4: 5-55233263-G-C
MyVariant Identifiers: chr5:g.54529091G>C (hg19) chr5:g.55233263G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233263G>C , CM000667.2:g.55233263G>C GRCh38
NC_000005.9:g.54529091G>C , CM000667.1:g.54529091G>C GRCh37
NC_000005.8:g.54564848G>C NCBI36
NG_034201.1:g.5455C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.261C>G MANE Select ENSP00000282572.4:p.Ala87=
ENST00000282572.4:c.261C>G ENSP00000282572.4:p.Ala87=
ENST00000501463.2:c.261C>G ENSP00000422485.1:p.Ala87=
NM_021147.4:c.261C>G NP_066970.3:p.Ala87=
NR_125346.1:n.455C>G
NR_125347.1:n.455C>G
NM_021147.5:c.261C>G MANE Select NP_066970.3:p.Ala87=
NR_125346.2:n.346C>G
NR_125347.2:n.346C>G
Search 100 bp 5'
Search 100 bp 3'