Canonical Allele Identifier: CA2254006455
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27764899G= , CM000679.2:g.27764899G= GRCh38
NC_000017.10:g.26091925G= , CM000679.1:g.26091925G= GRCh37
NC_000017.9:g.23116052G= NCBI36
NG_011470.1:g.40631C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.*3092+708C= ENSP00000513259.1:n.*3092+708C=
ENST00000697338.1:c.2276+636C= ENSP00000513260.1:n.2276+636C=
ENST00000697339.1:c.1390+708C= ENSP00000513261.1:n.1390+708C=
ENST00000697340.1:c.*1145+636C= ENSP00000513262.1:n.*1145+636C=
ENST00000697341.1:n.2398+636C=
ENST00000313735.11:c.2428+636C= MANE Select ENSP00000327251.6:n.2428+636C=
ENST00000646938.1:c.2425+636C= ENSP00000494870.1:n.2425+636C=
ENST00000313735.10:c.2428+636C= ENSP00000327251.6:n.2428+636C=
ENST00000621962.1:c.2311+636C= ENSP00000482291.1:n.2311+636C=
NM_000625.4:c.2428+636C= MANE Select NP_000616.3:n.2428+636C=
XM_011524859.1:c.2428+636C= XP_011523161.1:n.2428+636C=
XM_011524860.1:c.2425+636C= XP_011523162.1:n.2425+636C=
XM_011524861.1:c.2356+708C= XP_011523163.1:n.2356+708C=
XM_011524862.1:c.1762+636C= XP_011523164.1:n.1762+636C=