Canonical Allele Identifier: CA578703936

Gene: NOS3

Linked Data

• dbSNP Id: rs1307299387
• gnomAD v2: 7-150700892-A-G
• gnomAD v3: 7-151003804-A-G
• gnomAD v4: 7-151003804-A-G
• MyVariant Identifiers: chr7:g.150700892A>G (hg19) ; chr7:g.151003804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151003804A>G , CM000669.2:g.151003804A>G	GRCh38
NC_000007.13:g.150700892A>G , CM000669.1:g.150700892A>G	GRCh37
NC_000007.12:g.150331825A>G	NCBI36
NG_011992.1:g.17746A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1752+1500A>G MANE Select	ENSP00000297494.3:n.1752+1500A>G
ENST00000297494.7:c.1752+1500A>G	ENSP00000297494.3:n.1752+1500A>G
ENST00000461406.5:c.1134+1500A>G	ENSP00000417143.1:n.1134+1500A>G
ENST00000467517.1:c.2246A>G	ENSP00000420551.1:n.2246A>G
ENST00000484524.5:c.2406A>G	ENSP00000420215.1:n.2406A>G
NM_000603.4:c.1752+1500A>G	NP_000594.2:n.1752+1500A>G
NM_001160109.1:c.1900A>G	NP_001153581.1:n.1900A>G
NM_001160110.1:c.2246A>G	NP_001153582.1:n.2246A>G
NM_001160111.1:c.2406A>G	NP_001153583.1:n.2406A>G
XM_006716002.2:c.1752+1500A>G	XP_006716065.1:n.1752+1500A>G
NM_000603.5:c.1752+1500A>G MANE Select	NP_000594.2:n.1752+1500A>G
NM_001160109.2:c.*109A>G	NP_001153581.1:n.*109A>G