Canonical Allele Identifier: CA1752466996

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992463T= , CM000669.2:g.150992463T=	GRCh38
NC_000007.13:g.150689551T= , CM000669.1:g.150689551T=	GRCh37
NC_000007.12:g.150320484T=	NCBI36
NG_011992.1:g.6405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-52+1163T= MANE Select	ENSP00000297494.3:n.-52+1163T=
ENST00000297494.7:c.-52+1163T=	ENSP00000297494.3:n.-52+1163T=
ENST00000461406.5:c.-149+1163T=	ENSP00000417143.1:n.-149+1163T=
NM_000603.4:c.-52+1163T=	NP_000594.2:n.-52+1163T=
NM_000603.5:c.-52+1163T= MANE Select	NP_000594.2:n.-52+1163T=