Canonical Allele Identifier: CA1752467141

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992742G= , CM000669.2:g.150992742G=	GRCh38
NC_000007.13:g.150689830G= , CM000669.1:g.150689830G=	GRCh37
NC_000007.12:g.150320763G=	NCBI36
NG_011992.1:g.6684G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1011G= MANE Select	ENSP00000297494.3:n.-51-1011G=
ENST00000297494.7:c.-51-1011G=	ENSP00000297494.3:n.-51-1011G=
ENST00000461406.5:c.-149+1442G=	ENSP00000417143.1:n.-149+1442G=
NM_000603.4:c.-51-1011G=	NP_000594.2:n.-51-1011G=
NM_000603.5:c.-51-1011G= MANE Select	NP_000594.2:n.-51-1011G=