Canonical Allele Identifier: CA244252377
Gene: NOS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1004356

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339567T>C , CM000674.2:g.117339567T>C GRCh38
NC_000012.11:g.117777372T>C , CM000674.1:g.117777372T>C GRCh37
NC_000012.10:g.116261755T>C NCBI36
NG_011991.2:g.27211A>G

Transcript Alleles

HGVS Amino-acid change
NM_000620.4:c.-420-8078A>G VV NP_000611.1:p.=
NM_001204218.1:c.-420-8078A>G VV NP_001191147.1:p.=
XM_011538398.1:c.-420-8078A>G XP_011536700.1:p.=
NM_000620.5:c.-420-8078A>G VV MANE Preferred NP_000611.1:p.=
ENST00000317775.10:c.-420-8078A>G ENSP00000320758.6:p.=
ENST00000549189.1:n.471-8078A>G
ENST00000618760.4:c.-420-8078A>G ENSP00000477999.1:p.=