Canonical Allele Identifier: CA118944812
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs929986505
MyVariant Identifiers: chr5:g.54528903C>A (hg19) chr5:g.55233075C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233075C>A , CM000667.2:g.55233075C>A GRCh38
NC_000005.9:g.54528903C>A , CM000667.1:g.54528903C>A GRCh37
NC_000005.8:g.54564660C>A NCBI36
NG_034201.1:g.5643G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+68G>T MANE Select ENSP00000282572.4:n.381+68G>T
ENST00000282572.4:c.381+68G>T ENSP00000282572.4:n.381+68G>T
ENST00000501463.2:c.*53G>T ENSP00000422485.1:n.*53G>T
NM_021147.4:c.381+68G>T NP_066970.3:n.381+68G>T
NR_125346.1:n.643G>T
NR_125347.1:n.580+63G>T
NM_021147.5:c.381+68G>T MANE Select NP_066970.3:n.381+68G>T
NR_125346.2:n.534G>T
NR_125347.2:n.471+63G>T
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