Canonical Allele Identifier: CA399966582
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54672136C>G (hg19) chr17:g.56594775C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594775C>G , CM000679.2:g.56594775C>G GRCh38
NC_000017.10:g.54672136C>G , CM000679.1:g.54672136C>G GRCh37
NC_000017.9:g.52027135C>G NCBI36
NG_011958.1:g.6077C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.552C>G MANE Select ENSP00000328181.4:p.Cys184Trp
ENST00000332822.4:c.552C>G ENSP00000328181.4:p.Cys184Trp
NM_005450.4:c.552C>G NP_005441.1:p.Cys184Trp
NM_005450.6:c.552C>G MANE Select NP_005441.1:p.Cys184Trp
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Search 100 bp 3'