Canonical Allele Identifier: CA1604701084
Gene: CNOT6 HGNC NCBI

Linked Data

dbSNP Id: rs1561673226
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180578360A>G , CM000667.2:g.180578360A>G GRCh38
NC_000005.9:g.180005360A>G , CM000667.1:g.180005360A>G GRCh37
NC_000005.8:g.179937966A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393356.5:c.*4160A>G ENSP00000377024.1:n.*4160A>G
NM_001303241.1:c.*4160A>G NP_001290170.1:n.*4160A>G
NM_001303241.2:c.*4160A>G NP_001290170.1:n.*4160A>G
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