Canonical Allele Identifier: CA1604701089
Gene: CNOT6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180578363G= , CM000667.2:g.180578363G= GRCh38
NC_000005.9:g.180005363G= , CM000667.1:g.180005363G= GRCh37
NC_000005.8:g.179937969G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393356.5:c.*4163G= ENSP00000377024.1:n.*4163G=
NM_001303241.1:c.*4163G= NP_001290170.1:n.*4163G=
NM_001303241.2:c.*4163G= NP_001290170.1:n.*4163G=