Canonical Allele Identifier: CA808412486
Gene: CNOT6 HGNC NCBI

Linked Data

dbSNP Id: rs1220923490
MyVariant Identifiers: chr5:g.180005361T>C (hg19) chr5:g.180578361T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180578361T>C , CM000667.2:g.180578361T>C GRCh38
NC_000005.9:g.180005361T>C , CM000667.1:g.180005361T>C GRCh37
NC_000005.8:g.179937967T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393356.5:c.*4161T>C ENSP00000377024.1:n.*4161T>C
NM_001303241.1:c.*4161T>C NP_001290170.1:n.*4161T>C
NM_001303241.2:c.*4161T>C NP_001290170.1:n.*4161T>C
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