Canonical Allele Identifier: CA359724666
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233271-C-T
MyVariant Identifiers: chr5:g.54529099C>T (hg19) chr5:g.55233271C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233271C>T , CM000667.2:g.55233271C>T GRCh38
NC_000005.9:g.54529099C>T , CM000667.1:g.54529099C>T GRCh37
NC_000005.8:g.54564856C>T NCBI36
NG_034201.1:g.5447G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.253G>A MANE Select ENSP00000282572.4:p.Gly85Ser
ENST00000282572.4:c.253G>A ENSP00000282572.4:p.Gly85Ser
ENST00000501463.2:c.253G>A ENSP00000422485.1:p.Gly85Ser
NM_021147.4:c.253G>A NP_066970.3:p.Gly85Ser
NR_125346.1:n.447G>A
NR_125347.1:n.447G>A
NM_021147.5:c.253G>A MANE Select NP_066970.3:p.Gly85Ser
NR_125346.2:n.338G>A
NR_125347.2:n.338G>A
Search 100 bp 5'
Search 100 bp 3'