Canonical Allele Identifier: CA2066004766
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1593015446
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117313582C>T , CM000674.2:g.117313582C>T GRCh38
NC_000012.11:g.117751387C>T , CM000674.1:g.117751387C>T GRCh37
NC_000012.10:g.116235770C>T NCBI36
NG_011991.2:g.53196G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317775.11:c.726-1990G>A MANE Select ENSP00000320758.6:n.726-1990G>A
ENST00000317775.10:c.726-1990G>A ENSP00000320758.6:n.726-1990G>A
ENST00000338101.8:c.726-1990G>A ENSP00000337459.4:n.726-1990G>A
ENST00000344089.4:c.723-1990G>A ENSP00000339862.4:n.723-1990G>A
ENST00000618760.4:c.726-1990G>A ENSP00000477999.1:n.726-1990G>A
NM_000620.4:c.726-1990G>A NP_000611.1:n.726-1990G>A
NM_001204218.1:c.726-1990G>A NP_001191147.1:n.726-1990G>A
XM_011538398.1:c.726-1990G>A XP_011536700.1:n.726-1990G>A
NM_000620.5:c.726-1990G>A MANE Select NP_000611.1:n.726-1990G>A
NM_001204218.2:c.726-1990G>A NP_001191147.1:n.726-1990G>A
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