Canonical Allele Identifier: CA1752466989

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992451C= , CM000669.2:g.150992451C=	GRCh38
NC_000007.13:g.150689539C= , CM000669.1:g.150689539C=	GRCh37
NC_000007.12:g.150320472C=	NCBI36
NG_011992.1:g.6393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-52+1151C= MANE Select	ENSP00000297494.3:n.-52+1151C=
ENST00000297494.7:c.-52+1151C=	ENSP00000297494.3:n.-52+1151C=
ENST00000461406.5:c.-149+1151C=	ENSP00000417143.1:n.-149+1151C=
NM_000603.4:c.-52+1151C=	NP_000594.2:n.-52+1151C=
NM_000603.5:c.-52+1151C= MANE Select	NP_000594.2:n.-52+1151C=