Canonical Allele Identifier: CA579076082

Gene: NOS3

Linked Data

• dbSNP Id: rs1483344971
• gnomAD v2: 7-150698621-T-A
• gnomAD v4: 7-151001533-T-A
• MyVariant Identifiers: chr7:g.150698621T>A (hg19) ; chr7:g.151001533T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001533T>A , CM000669.2:g.151001533T>A	GRCh38
NC_000007.13:g.150698621T>A , CM000669.1:g.150698621T>A	GRCh37
NC_000007.12:g.150329554T>A	NCBI36
NG_011992.1:g.15475T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1429-11T>A MANE Select	ENSP00000297494.3:n.1429-11T>A
ENST00000297494.7:c.1429-11T>A	ENSP00000297494.3:n.1429-11T>A
ENST00000461406.5:c.811-11T>A	ENSP00000417143.1:n.811-11T>A
ENST00000467517.1:c.1429-11T>A	ENSP00000420551.1:n.1429-11T>A
ENST00000484524.5:c.1429-11T>A	ENSP00000420215.1:n.1429-11T>A
NM_000603.4:c.1429-11T>A	NP_000594.2:n.1429-11T>A
NM_001160109.1:c.1429-11T>A	NP_001153581.1:n.1429-11T>A
NM_001160110.1:c.1429-11T>A	NP_001153582.1:n.1429-11T>A
NM_001160111.1:c.1429-11T>A	NP_001153583.1:n.1429-11T>A
XM_006716002.2:c.1429-11T>A	XP_006716065.1:n.1429-11T>A
NM_000603.5:c.1429-11T>A MANE Select	NP_000594.2:n.1429-11T>A
NM_001160109.2:c.1429-11T>A	NP_001153581.1:n.1429-11T>A