Canonical Allele Identifier: CA398316980

Gene: NOS2

Linked Data

• gnomAD v4: 17-27804206-C-T
• MyVariant Identifiers: chr17:g.26131232C>T (hg19) ; chr17:g.27804206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27804206C>T , CM000679.2:g.27804206C>T	GRCh38
NC_000017.10:g.26131232C>T , CM000679.1:g.26131232C>T	GRCh37
NC_000017.9:g.23155359C>T	NCBI36
NG_011470.1:g.1324G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000582441.1:c.355G>A	ENSP00000462879.1:p.Gly119Arg
XM_011524859.1:c.-157G>A	XP_011523161.1:n.-157G>A