Canonical Allele Identifier: CA1752467075
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992617C= , CM000669.2:g.150992617C= GRCh38
NC_000007.13:g.150689705C= , CM000669.1:g.150689705C= GRCh37
NC_000007.12:g.150320638C= NCBI36
NG_011992.1:g.6559C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-1136C= MANE Select ENSP00000297494.3:n.-51-1136C=
ENST00000297494.7:c.-51-1136C= ENSP00000297494.3:n.-51-1136C=
ENST00000461406.5:c.-149+1317C= ENSP00000417143.1:n.-149+1317C=
NM_000603.4:c.-51-1136C= NP_000594.2:n.-51-1136C=
NM_000603.5:c.-51-1136C= MANE Select NP_000594.2:n.-51-1136C=