Canonical Allele Identifier: CA1752442162
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151001935G= , CM000669.2:g.151001935G= GRCh38
NC_000007.13:g.150699023G= , CM000669.1:g.150699023G= GRCh37
NC_000007.12:g.150329956G= NCBI36
NG_011992.1:g.15877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.1617G= MANE Select ENSP00000297494.3:p.Gly539=
ENST00000297494.7:c.1617G= ENSP00000297494.3:p.Gly539=
ENST00000460603.1:n.69G=
ENST00000461406.5:c.999G= ENSP00000417143.1:p.Gly333=
ENST00000467517.1:c.1617G= ENSP00000420551.1:p.Gly539=
ENST00000484524.5:c.1617G= ENSP00000420215.1:p.Gly539=
NM_000603.4:c.1617G= NP_000594.2:p.Gly539=
NM_001160109.1:c.1617G= NP_001153581.1:p.Gly539=
NM_001160110.1:c.1617G= NP_001153582.1:p.Gly539=
NM_001160111.1:c.1617G= NP_001153583.1:p.Gly539=
XM_006716002.2:c.1617G= XP_006716065.1:p.Gly539=
NM_000603.5:c.1617G= MANE Select NP_000594.2:p.Gly539=
NM_001160109.2:c.1617G= NP_001153581.1:p.Gly539=