Canonical Allele Identifier: CA133213906
Gene: CNOT6 HGNC NCBI

Linked Data

dbSNP Id: rs571364955
gnomAD v3: 5-180578363-G-C
gnomAD v4: 5-180578363-G-C
MyVariant Identifiers: chr5:g.180005363G>C (hg19) chr5:g.180578363G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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