Canonical Allele Identifier: CA13730128
Gene: NOS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2682826

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117215033G>A , CM000674.2:g.117215033G>A GRCh38
NC_000012.11:g.117652838G>A , CM000674.1:g.117652838G>A GRCh37
NC_000012.10:g.116137221G>A NCBI36
NG_011991.2:g.151745C>T

Transcript Alleles

HGVS Amino-acid change
NM_000620.4:c.*276C>T VV NP_000611.1:p.=
NM_001204213.1:c.*276C>T VV NP_001191142.1:p.=
NM_001204214.1:c.*276C>T VV NP_001191143.1:p.=
NM_001204218.1:c.*276C>T VV NP_001191147.1:p.=
XM_011538398.1:c.*276C>T XP_011536700.1:p.=
NM_000620.5:c.*276C>T VV MANE Preferred NP_000611.1:p.=
ENST00000317775.10:c.*276C>T ENSP00000320758.6:p.=
ENST00000618760.4:c.*276C>T ENSP00000477999.1:p.=