Canonical Allele Identifier: CA359724490
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1425150391
gnomAD v2: 5-54529070-A-C
gnomAD v4: 5-55233242-A-C
MyVariant Identifiers: chr5:g.54529070A>C (hg19) chr5:g.55233242A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233242A>C , CM000667.2:g.55233242A>C GRCh38
NC_000005.9:g.54529070A>C , CM000667.1:g.54529070A>C GRCh37
NC_000005.8:g.54564827A>C NCBI36
NG_034201.1:g.5476T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.282T>G MANE Select ENSP00000282572.4:p.Asp94Glu
ENST00000282572.4:c.282T>G ENSP00000282572.4:p.Asp94Glu
ENST00000501463.2:c.282T>G ENSP00000422485.1:p.Asp94Glu
NM_021147.4:c.282T>G NP_066970.3:p.Asp94Glu
NR_125346.1:n.476T>G
NR_125347.1:n.476T>G
NM_021147.5:c.282T>G MANE Select NP_066970.3:p.Asp94Glu
NR_125346.2:n.367T>G
NR_125347.2:n.367T>G
Search 100 bp 5'
Search 100 bp 3'