Canonical Allele Identifier: CA2066032905
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1875995792

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339491C>A , CM000674.2:g.117339491C>A GRCh38
NC_000012.11:g.117777296C>A , CM000674.1:g.117777296C>A GRCh37
NC_000012.10:g.116261679C>A NCBI36
NG_011991.2:g.27287G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-8002G>T MANE Select ENSP00000320758.6:n.-420-8002G>T
ENST00000317775.10:c.-420-8002G>T ENSP00000320758.6:n.-420-8002G>T
ENST00000549189.1:n.471-8002G>T
ENST00000618760.4:c.-420-8002G>T ENSP00000477999.1:n.-420-8002G>T
NM_000620.4:c.-420-8002G>T NP_000611.1:n.-420-8002G>T
NM_001204218.1:c.-420-8002G>T NP_001191147.1:n.-420-8002G>T
XM_011538398.1:c.-420-8002G>T XP_011536700.1:n.-420-8002G>T
NM_000620.5:c.-420-8002G>T MANE Select NP_000611.1:n.-420-8002G>T
NM_001204218.2:c.-420-8002G>T NP_001191147.1:n.-420-8002G>T