Canonical Allele Identifier: CA1752460168
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010904C= , CM000669.2:g.151010904C= GRCh38
NC_000007.13:g.150707992C= , CM000669.1:g.150707992C= GRCh37
NC_000007.12:g.150338925C= NCBI36
NG_011992.1:g.24846C=
NG_030317.1:g.18596G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2902C= MANE Select ENSP00000297494.3:p.Leu968=
ENST00000297494.7:c.2902C= ENSP00000297494.3:p.Leu968=
ENST00000461406.5:c.2284C= ENSP00000417143.1:p.Leu762=
ENST00000468293.5:n.385C=
ENST00000475017.1:c.783C=
ENST00000477227.1:n.281C=
NM_000603.4:c.2902C= NP_000594.2:p.Leu968=
NM_000603.5:c.2902C= MANE Select NP_000594.2:p.Leu968=