Canonical Allele Identifier: CA359725352
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233370-G-T
MyVariant Identifiers: chr5:g.54529198G>T (hg19) chr5:g.55233370G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233370G>T , CM000667.2:g.55233370G>T GRCh38
NC_000005.9:g.54529198G>T , CM000667.1:g.54529198G>T GRCh37
NC_000005.8:g.54564955G>T NCBI36
NG_034201.1:g.5348C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.154C>A MANE Select ENSP00000282572.4:p.Pro52Thr
ENST00000282572.4:c.154C>A ENSP00000282572.4:p.Pro52Thr
ENST00000501463.2:c.154C>A ENSP00000422485.1:p.Pro52Thr
NM_021147.4:c.154C>A NP_066970.3:p.Pro52Thr
NR_125346.1:n.348C>A
NR_125347.1:n.348C>A
NM_021147.5:c.154C>A MANE Select NP_066970.3:p.Pro52Thr
NR_125346.2:n.239C>A
NR_125347.2:n.239C>A
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