Canonical Allele Identifier: CA169098087

Gene: NOS3

Linked Data

• dbSNP Id: rs1800783
• gnomAD v2: 7-150689397-A-C
• gnomAD v3: 7-150992309-A-C
• gnomAD v4: 7-150992309-A-C
• MyVariant Identifiers: chr7:g.150689397A>C (hg19) ; chr7:g.150992309A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992309A>C , CM000669.2:g.150992309A>C	GRCh38
NC_000007.13:g.150689397A>C , CM000669.1:g.150689397A>C	GRCh37
NC_000007.12:g.150320330A>C	NCBI36
NG_011992.1:g.6251A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.-52+1009A>C MANE Select	ENSP00000297494.3:n.-52+1009A>C
ENST00000297494.7:c.-52+1009A>C	ENSP00000297494.3:n.-52+1009A>C
ENST00000461406.5:c.-149+1009A>C	ENSP00000417143.1:n.-149+1009A>C
NM_000603.4:c.-52+1009A>C	NP_000594.2:n.-52+1009A>C
NM_000603.5:c.-52+1009A>C MANE Select	NP_000594.2:n.-52+1009A>C