Canonical Allele Identifier: CA444396869
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233233-G-A
MyVariant Identifiers: chr5:g.54529061G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233233G>A , CM000667.2:g.55233233G>A GRCh38
NC_000005.9:g.54529061G>A , CM000667.1:g.54529061G>A GRCh37
NC_000005.8:g.54564818G>A NCBI36
NG_034201.1:g.5485C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.291C>T MANE Select ENSP00000282572.4:p.Thr97=
ENST00000282572.4:c.291C>T ENSP00000282572.4:p.Thr97=
ENST00000501463.2:c.291C>T ENSP00000422485.1:p.Thr97=
NM_021147.4:c.291C>T NP_066970.3:p.Thr97=
NR_125346.1:n.485C>T
NR_125347.1:n.485C>T
NM_021147.5:c.291C>T MANE Select NP_066970.3:p.Thr97=
NR_125346.2:n.376C>T
NR_125347.2:n.376C>T