Canonical Allele Identifier: CA2066005346

Gene: NOS1

Linked Data

• dbSNP Id: rs1874580891

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117314371C>T , CM000674.2:g.117314371C>T	GRCh38
NC_000012.11:g.117752176C>T , CM000674.1:g.117752176C>T	GRCh37
NC_000012.10:g.116236559C>T	NCBI36
NG_011991.2:g.52407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.726-2779G>A MANE Select	ENSP00000320758.6:n.726-2779G>A
ENST00000317775.10:c.726-2779G>A	ENSP00000320758.6:n.726-2779G>A
ENST00000338101.8:c.726-2779G>A	ENSP00000337459.4:n.726-2779G>A
ENST00000344089.4:c.723-2779G>A	ENSP00000339862.4:n.723-2779G>A
ENST00000618760.4:c.726-2779G>A	ENSP00000477999.1:n.726-2779G>A
NM_000620.4:c.726-2779G>A	NP_000611.1:n.726-2779G>A
NM_001204218.1:c.726-2779G>A	NP_001191147.1:n.726-2779G>A
XM_011538398.1:c.726-2779G>A	XP_011536700.1:n.726-2779G>A
NM_000620.5:c.726-2779G>A MANE Select	NP_000611.1:n.726-2779G>A
NM_001204218.2:c.726-2779G>A	NP_001191147.1:n.726-2779G>A