Canonical Allele Identifier: CA2254004732

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27760941T= , CM000679.2:g.27760941T=	GRCh38
NC_000017.10:g.26087967T= , CM000679.1:g.26087967T=	GRCh37
NC_000017.9:g.23112094T=	NCBI36
NG_011470.1:g.44589A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000625.4:c.2889-197A= MANE Select	NP_000616.3:n.2889-197A=
ENST00000313735.11:c.2889-197A= MANE Select	ENSP00000327251.6:n.2889-197A=
ENST00000313735.10:c.2889-197A=	ENSP00000327251.6:n.2889-197A=
ENST00000621962.1:c.2772-197A=	ENSP00000482291.1:n.2772-197A=
ENST00000646938.1:c.2886-197A=	ENSP00000494870.1:n.2886-197A=
ENST00000697337.1:c.*3553-197A=	ENSP00000513259.1:n.*3553-197A=
ENST00000697338.1:c.2737-197A=	ENSP00000513260.1:n.2737-197A=
ENST00000697339.1:c.1851-197A=	ENSP00000513261.1:n.1851-197A=
ENST00000697340.1:c.*1602-197A=	ENSP00000513262.1:n.*1602-197A=
XM_011524859.1:c.2889-197A=	XP_011523161.1:n.2889-197A=
XM_011524860.1:c.2886-197A=	XP_011523162.1:n.2886-197A=
XM_011524861.1:c.2817-197A=	XP_011523163.1:n.2817-197A=
XM_011524862.1:c.2223-197A=	XP_011523164.1:n.2223-197A=