Canonical Allele Identifier: CA684125622
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1052098967

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117339569C>G , CM000674.2:g.117339569C>G GRCh38
NC_000012.11:g.117777374C>G , CM000674.1:g.117777374C>G GRCh37
NC_000012.10:g.116261757C>G NCBI36
NG_011991.2:g.27209G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-8080G>C MANE Select ENSP00000320758.6:n.-420-8080G>C
ENST00000317775.10:c.-420-8080G>C ENSP00000320758.6:n.-420-8080G>C
ENST00000549189.1:n.471-8080G>C
ENST00000618760.4:c.-420-8080G>C ENSP00000477999.1:n.-420-8080G>C
NM_000620.4:c.-420-8080G>C NP_000611.1:n.-420-8080G>C
NM_001204218.1:c.-420-8080G>C NP_001191147.1:n.-420-8080G>C
XM_011538398.1:c.-420-8080G>C XP_011536700.1:n.-420-8080G>C
NM_000620.5:c.-420-8080G>C MANE Select NP_000611.1:n.-420-8080G>C
NM_001204218.2:c.-420-8080G>C NP_001191147.1:n.-420-8080G>C