Canonical Allele Identifier: CA1752467213
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1802285572
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992918C>A , CM000669.2:g.150992918C>A GRCh38
NC_000007.13:g.150690006C>A , CM000669.1:g.150690006C>A GRCh37
NC_000007.12:g.150320939C>A NCBI36
NG_011992.1:g.6860C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-835C>A MANE Select ENSP00000297494.3:n.-51-835C>A
ENST00000297494.7:c.-51-835C>A ENSP00000297494.3:n.-51-835C>A
ENST00000461406.5:c.-149+1618C>A ENSP00000417143.1:n.-149+1618C>A
NM_000603.4:c.-51-835C>A NP_000594.2:n.-51-835C>A
NM_000603.5:c.-51-835C>A MANE Select NP_000594.2:n.-51-835C>A
Search 100 bp 5'
Search 100 bp 3'