Canonical Allele Identifier: CA169098137

Gene: NOS3

Linked Data

• dbSNP Id: rs34417010

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992452dup , CM000669.2:g.150992452dup	GRCh38
NC_000007.13:g.150689540dup , CM000669.1:g.150689540dup	GRCh37
NC_000007.12:g.150320473dup	NCBI36
NG_011992.1:g.6394dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-52+1152dup MANE Select	ENSP00000297494.3:n.-52+1152dup
ENST00000297494.7:c.-52+1152dup	ENSP00000297494.3:n.-52+1152dup
ENST00000461406.5:c.-149+1152dup	ENSP00000417143.1:n.-149+1152dup
NM_000603.4:c.-52+1152dup	NP_000594.2:n.-52+1152dup
NM_000603.5:c.-52+1152dup MANE Select	NP_000594.2:n.-52+1152dup