Canonical Allele Identifier: CA12525506

Gene: NOS3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992855G>A , CM000669.2:g.150992855G>A	GRCh38
NC_000007.13:g.150689943G>A , CM000669.1:g.150689943G>A	GRCh37
NC_000007.12:g.150320876G>A	NCBI36
NG_011992.1:g.6797G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-898G>A MANE Select	ENSP00000297494.3:n.-51-898G>A
ENST00000297494.7:c.-51-898G>A	ENSP00000297494.3:n.-51-898G>A
ENST00000461406.5:c.-149+1555G>A	ENSP00000417143.1:n.-149+1555G>A
NM_000603.4:c.-51-898G>A	NP_000594.2:n.-51-898G>A
NM_000603.5:c.-51-898G>A MANE Select	NP_000594.2:n.-51-898G>A