Canonical Allele Identifier: CA1604701091
Gene: CNOT6 HGNC NCBI

Linked Data

dbSNP Id: rs1761099164
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180578365G>A , CM000667.2:g.180578365G>A GRCh38
NC_000005.9:g.180005365G>A , CM000667.1:g.180005365G>A GRCh37
NC_000005.8:g.179937971G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393356.5:c.*4165G>A ENSP00000377024.1:n.*4165G>A
NM_001303241.1:c.*4165G>A NP_001290170.1:n.*4165G>A
NM_001303241.2:c.*4165G>A NP_001290170.1:n.*4165G>A
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