Canonical Allele Identifier: CA12488582
Gene: NOS3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 517660
ClinVar RCV Id: RCV000678037
dbSNP Id: rs2070744

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992991C>T , CM000669.2:g.150992991C>T GRCh38
NC_000007.12:g.150321012C>T NCBI36
NC_000007.13:g.150690079C>T , CM000669.1:g.150690079C>T GRCh37
NG_011992.1:g.6933C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.7:c.-51-762C>T ENSP00000297494.3:p.=
ENST00000461406.5:c.-149+1691C>T ENSP00000417143.1:p.=
NM_000603.4:c.-51-762C>T VV NP_000594.2:p.=