Canonical Allele Identifier: CA399966016

Gene: NOG

Linked Data

• dbSNP Id: rs2052470497
• gnomAD v3: 17-56594617-G-A
• gnomAD v4: 17-56594617-G-A
• MyVariant Identifiers: chr17:g.54671978G>A (hg19) ; chr17:g.56594617G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594617G>A , CM000679.2:g.56594617G>A	GRCh38
NC_000017.10:g.54671978G>A , CM000679.1:g.54671978G>A	GRCh37
NC_000017.9:g.52026977G>A	NCBI36
NG_011958.1:g.5919G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.394G>A MANE Select	ENSP00000328181.4:p.Gly132Ser
ENST00000332822.4:c.394G>A	ENSP00000328181.4:p.Gly132Ser
NM_005450.4:c.394G>A	NP_005441.1:p.Gly132Ser
NM_005450.6:c.394G>A MANE Select	NP_005441.1:p.Gly132Ser