Canonical Allele Identifier: CA2254008189

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769300C= , CM000679.2:g.27769300C=	GRCh38
NC_000017.10:g.26096326C= , CM000679.1:g.26096326C=	GRCh37
NC_000017.9:g.23120453C=	NCBI36
NG_011470.1:g.36230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2596-149G=	ENSP00000513259.1:n.*2596-149G=
ENST00000697338.1:c.1708-149G=	ENSP00000513260.1:n.1708-149G=
ENST00000697339.1:c.894-149G=	ENSP00000513261.1:n.894-149G=
ENST00000697340.1:c.*577-149G=	ENSP00000513262.1:n.*577-149G=
ENST00000697341.1:n.1830-149G=
ENST00000313735.11:c.1860-149G= MANE Select	ENSP00000327251.6:n.1860-149G=
ENST00000646938.1:c.1857-149G=	ENSP00000494870.1:n.1857-149G=
ENST00000313735.10:c.1860-149G=	ENSP00000327251.6:n.1860-149G=
ENST00000621962.1:c.1743-149G=	ENSP00000482291.1:n.1743-149G=
NM_000625.4:c.1860-149G= MANE Select	NP_000616.3:n.1860-149G=
XM_011524859.1:c.1860-149G=	XP_011523161.1:n.1860-149G=
XM_011524860.1:c.1857-149G=	XP_011523162.1:n.1857-149G=
XM_011524861.1:c.1860-149G=	XP_011523163.1:n.1860-149G=
XM_011524862.1:c.1194-149G=	XP_011523164.1:n.1194-149G=