Canonical Allele Identifier: CA1108714776

Gene: NOS3

Linked Data

• dbSNP Id: rs1802286526
• gnomAD v3: 7-150992968-A-G
• gnomAD v4: 7-150992968-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992968A>G , CM000669.2:g.150992968A>G	GRCh38
NC_000007.13:g.150690056A>G , CM000669.1:g.150690056A>G	GRCh37
NC_000007.12:g.150320989A>G	NCBI36
NG_011992.1:g.6910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-785A>G MANE Select	ENSP00000297494.3:n.-51-785A>G
ENST00000297494.7:c.-51-785A>G	ENSP00000297494.3:n.-51-785A>G
ENST00000461406.5:c.-149+1668A>G	ENSP00000417143.1:n.-149+1668A>G
NM_000603.4:c.-51-785A>G	NP_000594.2:n.-51-785A>G
NM_000603.5:c.-51-785A>G MANE Select	NP_000594.2:n.-51-785A>G