Canonical Allele Identifier: CA2254014137
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27782024C= , CM000679.2:g.27782024C= GRCh38
NC_000017.10:g.26109050C= , CM000679.1:g.26109050C= GRCh37
NC_000017.9:g.23133177C= NCBI36
NG_011470.1:g.23506G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*159G= ENSP00000513259.1:n.*159G=
ENST00000697338.1:c.561G= ENSP00000513260.1:n.561G=
ENST00000697339.1:c.315+6785G= ENSP00000513261.1:n.315+6785G=
ENST00000697340.1:c.710G= ENSP00000513262.1:p.Gly237=
ENST00000697341.1:n.683G=
ENST00000313735.11:c.713G= MANE Select ENSP00000327251.6:p.Gly238=
ENST00000646938.1:c.710G= ENSP00000494870.1:p.Gly237=
ENST00000313735.10:c.713G= ENSP00000327251.6:p.Gly238=
ENST00000621962.1:c.713G= ENSP00000482291.1:p.Gly238=
NM_000625.4:c.713G= MANE Select NP_000616.3:p.Gly238=
XM_011524859.1:c.713G= XP_011523161.1:p.Gly238=
XM_011524860.1:c.710G= XP_011523162.1:p.Gly237=
XM_011524861.1:c.713G= XP_011523163.1:p.Gly238=
XM_011524862.1:c.47G= XP_011523164.1:p.Gly16=