Canonical Allele Identifier: CA2254009809
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27772192C= , CM000679.2:g.27772192C= GRCh38
NC_000017.10:g.26099218C= , CM000679.1:g.26099218C= GRCh37
NC_000017.9:g.23123345C= NCBI36
NG_011470.1:g.33338G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*1266G= ENSP00000513259.1:n.*1266G=
ENST00000697338.1:c.1552+116G= ENSP00000513260.1:n.1552+116G=
ENST00000697339.1:c.738+116G= ENSP00000513261.1:n.738+116G=
ENST00000697340.1:c.*421+116G= ENSP00000513262.1:n.*421+116G=
ENST00000697341.1:n.1674+116G=
ENST00000313735.11:c.1704+116G= MANE Select ENSP00000327251.6:n.1704+116G=
ENST00000646938.1:c.1701+116G= ENSP00000494870.1:n.1701+116G=
ENST00000313735.10:c.1704+116G= ENSP00000327251.6:n.1704+116G=
ENST00000621962.1:c.1587+116G= ENSP00000482291.1:n.1587+116G=
NM_000625.4:c.1704+116G= MANE Select NP_000616.3:n.1704+116G=
XM_011524859.1:c.1704+116G= XP_011523161.1:n.1704+116G=
XM_011524860.1:c.1701+116G= XP_011523162.1:n.1701+116G=
XM_011524861.1:c.1704+116G= XP_011523163.1:n.1704+116G=
XM_011524862.1:c.1038+116G= XP_011523164.1:n.1038+116G=