Canonical Allele Identifier: CA118945258
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1052951064
gnomAD v2: 5-54529148-T-G
gnomAD v4: 5-55233320-T-G
MyVariant Identifiers: chr5:g.54529148T>G (hg19) chr5:g.55233320T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233320T>G , CM000667.2:g.55233320T>G GRCh38
NC_000005.9:g.54529148T>G , CM000667.1:g.54529148T>G GRCh37
NC_000005.8:g.54564905T>G NCBI36
NG_034201.1:g.5398A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.204A>C MANE Select ENSP00000282572.4:p.Ser68=
ENST00000282572.4:c.204A>C ENSP00000282572.4:p.Ser68=
ENST00000501463.2:c.204A>C ENSP00000422485.1:p.Ser68=
NM_021147.4:c.204A>C NP_066970.3:p.Ser68=
NR_125346.1:n.398A>C
NR_125347.1:n.398A>C
NM_021147.5:c.204A>C MANE Select NP_066970.3:p.Ser68=
NR_125346.2:n.289A>C
NR_125347.2:n.289A>C
Search 100 bp 5'
Search 100 bp 3'