Canonical Allele Identifier: CA2727280482
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs2136073894
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117329811C>T , CM000674.2:g.117329811C>T GRCh38
NC_000012.11:g.117767616C>T , CM000674.1:g.117767616C>T GRCh37
NC_000012.10:g.116251999C>T NCBI36
NG_011991.2:g.36967G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.725+534G>A MANE Select ENSP00000320758.6:n.725+534G>A
ENST00000317775.10:c.725+534G>A ENSP00000320758.6:n.725+534G>A
ENST00000338101.8:c.725+534G>A ENSP00000337459.4:n.725+534G>A
ENST00000344089.4:c.722+534G>A ENSP00000339862.4:n.722+534G>A
ENST00000618760.4:c.725+534G>A ENSP00000477999.1:n.725+534G>A
NM_000620.4:c.725+534G>A NP_000611.1:n.725+534G>A
NM_001204218.1:c.725+534G>A NP_001191147.1:n.725+534G>A
XM_011538398.1:c.725+534G>A XP_011536700.1:n.725+534G>A
NM_000620.5:c.725+534G>A MANE Select NP_000611.1:n.725+534G>A
NM_001204218.2:c.725+534G>A NP_001191147.1:n.725+534G>A
Search 100 bp 5'
Search 100 bp 3'