Canonical Allele Identifier: CA1108714787
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1802286767
gnomAD v3: 7-150992989-G-A
gnomAD v4: 7-150992989-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992989G>A , CM000669.2:g.150992989G>A GRCh38
NC_000007.13:g.150690077G>A , CM000669.1:g.150690077G>A GRCh37
NC_000007.12:g.150321010G>A NCBI36
NG_011992.1:g.6931G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-764G>A MANE Select ENSP00000297494.3:n.-51-764G>A
ENST00000297494.7:c.-51-764G>A ENSP00000297494.3:n.-51-764G>A
ENST00000461406.5:c.-149+1689G>A ENSP00000417143.1:n.-149+1689G>A
NM_000603.4:c.-51-764G>A NP_000594.2:n.-51-764G>A
NM_000603.5:c.-51-764G>A MANE Select NP_000594.2:n.-51-764G>A
Search 100 bp 5'
Search 100 bp 3'