Canonical Allele Identifier: CA1752460176
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010906G= , CM000669.2:g.151010906G= GRCh38
NC_000007.13:g.150707994G= , CM000669.1:g.150707994G= GRCh37
NC_000007.12:g.150338927G= NCBI36
NG_011992.1:g.24848G=
NG_030317.1:g.18594C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2904G= MANE Select ENSP00000297494.3:p.Leu968=
ENST00000297494.7:c.2904G= ENSP00000297494.3:p.Leu968=
ENST00000461406.5:c.2286G= ENSP00000417143.1:p.Leu762=
ENST00000468293.5:n.387G=
ENST00000475017.1:c.785G=
ENST00000477227.1:n.283G=
NM_000603.4:c.2904G= NP_000594.2:p.Leu968=
NM_000603.5:c.2904G= MANE Select NP_000594.2:p.Leu968=