Canonical Allele Identifier: CA118945505
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1000117529
gnomAD v4: 5-55233517-T-G
MyVariant Identifiers: chr5:g.54529345T>G (hg19) chr5:g.55233517T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233517T>G , CM000667.2:g.55233517T>G GRCh38
NC_000005.9:g.54529345T>G , CM000667.1:g.54529345T>G GRCh37
NC_000005.8:g.54565102T>G NCBI36
NG_034201.1:g.5201A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.7A>C MANE Select ENSP00000282572.4:p.Thr3Pro
ENST00000282572.4:c.7A>C ENSP00000282572.4:p.Thr3Pro
ENST00000501463.2:c.7A>C ENSP00000422485.1:p.Thr3Pro
NM_021147.4:c.7A>C NP_066970.3:p.Thr3Pro
NR_125346.1:n.201A>C
NR_125347.1:n.201A>C
NM_021147.5:c.7A>C MANE Select NP_066970.3:p.Thr3Pro
NR_125346.2:n.92A>C
NR_125347.2:n.92A>C
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