Canonical Allele Identifier: CA626958040

Gene: NOG

Linked Data

• dbSNP Id: rs1325485297
• gnomAD v2: 17-54672391-A-C
• gnomAD v3: 17-56595030-A-C
• gnomAD v4: 17-56595030-A-C
• MyVariant Identifiers: chr17:g.54672391A>C (hg19) ; chr17:g.56595030A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595030A>C , CM000679.2:g.56595030A>C	GRCh38
NC_000017.10:g.54672391A>C , CM000679.1:g.54672391A>C	GRCh37
NC_000017.9:g.52027390A>C	NCBI36
NG_011958.1:g.6332A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*108A>C MANE Select	ENSP00000328181.4:n.*108A>C
ENST00000332822.4:c.*108A>C	ENSP00000328181.4:n.*108A>C
NM_005450.4:c.*108A>C	NP_005441.1:n.*108A>C
NM_005450.6:c.*108A>C MANE Select	NP_005441.1:n.*108A>C