Canonical Allele Identifier: CA1108714685

Gene: NOS3

Linked Data

• dbSNP Id: rs1243548554
• gnomAD v3: 7-150992637-A-C
• gnomAD v4: 7-150992637-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992637A>C , CM000669.2:g.150992637A>C	GRCh38
NC_000007.13:g.150689725A>C , CM000669.1:g.150689725A>C	GRCh37
NC_000007.12:g.150320658A>C	NCBI36
NG_011992.1:g.6579A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1116A>C MANE Select	ENSP00000297494.3:n.-51-1116A>C
ENST00000297494.7:c.-51-1116A>C	ENSP00000297494.3:n.-51-1116A>C
ENST00000461406.5:c.-149+1337A>C	ENSP00000417143.1:n.-149+1337A>C
NM_000603.4:c.-51-1116A>C	NP_000594.2:n.-51-1116A>C
NM_000603.5:c.-51-1116A>C MANE Select	NP_000594.2:n.-51-1116A>C