Canonical Allele Identifier: CA500753306
Gene: NOG HGNC NCBI

Linked Data

gnomAD v4: 17-56594232-C-G
MyVariant Identifiers: chr17:g.54671593C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594232C>G , CM000679.2:g.56594232C>G GRCh38
NC_000017.10:g.54671593C>G , CM000679.1:g.54671593C>G GRCh37
NC_000017.9:g.52026592C>G NCBI36
NG_011958.1:g.5534C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.9C>G MANE Select ENSP00000328181.4:p.Arg3=
ENST00000332822.4:c.9C>G ENSP00000328181.4:p.Arg3=
NM_005450.4:c.9C>G NP_005441.1:p.Arg3=
NM_005450.6:c.9C>G MANE Select NP_005441.1:p.Arg3=
Search 100 bp 5'
Search 100 bp 3'