Canonical Allele Identifier: CA399966530

Gene: NOG

Linked Data

• dbSNP Id: rs2052471473
• gnomAD v3: 17-56594753-G-A
• gnomAD v4: 17-56594753-G-A
• MyVariant Identifiers: chr17:g.54672114G>A (hg19) ; chr17:g.56594753G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594753G>A , CM000679.2:g.56594753G>A	GRCh38
NC_000017.10:g.54672114G>A , CM000679.1:g.54672114G>A	GRCh37
NC_000017.9:g.52027113G>A	NCBI36
NG_011958.1:g.6055G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.530G>A MANE Select	ENSP00000328181.4:p.Ser177Asn
ENST00000332822.4:c.530G>A	ENSP00000328181.4:p.Ser177Asn
NM_005450.4:c.530G>A	NP_005441.1:p.Ser177Asn
NM_005450.6:c.530G>A MANE Select	NP_005441.1:p.Ser177Asn