Canonical Allele Identifier: CA399965962
Gene: NOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.54671961C>A (hg19) chr17:g.56594600C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594600C>A , CM000679.2:g.56594600C>A GRCh38
NC_000017.10:g.54671961C>A , CM000679.1:g.54671961C>A GRCh37
NC_000017.9:g.52026960C>A NCBI36
NG_011958.1:g.5902C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332822.6:c.377C>A MANE Select ENSP00000328181.4:p.Ser126Tyr
ENST00000332822.4:c.377C>A ENSP00000328181.4:p.Ser126Tyr
NM_005450.4:c.377C>A NP_005441.1:p.Ser126Tyr
NM_005450.6:c.377C>A MANE Select NP_005441.1:p.Ser126Tyr
Search 100 bp 5'
Search 100 bp 3'