Canonical Allele Identifier: CA8663235
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs757867236

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594909A>G , CM000679.2:g.56594909A>G GRCh38
NC_000017.10:g.54672270A>G , CM000679.1:g.54672270A>G GRCh37
NC_000017.9:g.52027269A>G NCBI36
NG_011958.1:g.6211A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.686A>G MANE Select ENSP00000328181.4:p.Lys229Arg
ENST00000332822.4:c.686A>G ENSP00000328181.4:p.Lys229Arg
NM_005450.4:c.686A>G NP_005441.1:p.Lys229Arg
NM_005450.6:c.686A>G MANE Select NP_005441.1:p.Lys229Arg