Canonical Allele Identifier: CA244264883
Gene: NOS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11611788

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117300571T>C , CM000674.2:g.117300571T>C GRCh38
NC_000012.11:g.117738376T>C , CM000674.1:g.117738376T>C GRCh37
NC_000012.10:g.116222759T>C NCBI36
NG_011991.2:g.66207A>G

Transcript Alleles

HGVS Amino-acid change
NM_000620.4:c.853-10145A>G VV NP_000611.1:p.=
NM_001204213.1:c.-157+1445A>G VV NP_001191142.1:p.=
NM_001204214.1:c.-157+1445A>G VV NP_001191143.1:p.=
NM_001204218.1:c.853-10145A>G VV NP_001191147.1:p.=
XM_011538398.1:c.853-10145A>G XP_011536700.1:p.=
ENST00000317775.10:c.853-10145A>G ENSP00000320758.6:p.=
ENST00000338101.8:c.853-10145A>G ENSP00000337459.4:p.=
ENST00000344089.4:c.850-10145A>G ENSP00000339862.4:p.=
ENST00000618760.4:c.853-10145A>G ENSP00000477999.1:p.=