Canonical Allele Identifier: CA2254009801

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27772179C= , CM000679.2:g.27772179C=	GRCh38
NC_000017.10:g.26099205C= , CM000679.1:g.26099205C=	GRCh37
NC_000017.9:g.23123332C=	NCBI36
NG_011470.1:g.33351G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*1279G=	ENSP00000513259.1:n.*1279G=
ENST00000697338.1:c.1552+129G=	ENSP00000513260.1:n.1552+129G=
ENST00000697339.1:c.738+129G=	ENSP00000513261.1:n.738+129G=
ENST00000697340.1:c.*421+129G=	ENSP00000513262.1:n.*421+129G=
ENST00000697341.1:n.1674+129G=
ENST00000313735.11:c.1704+129G= MANE Select	ENSP00000327251.6:n.1704+129G=
ENST00000646938.1:c.1701+129G=	ENSP00000494870.1:n.1701+129G=
ENST00000313735.10:c.1704+129G=	ENSP00000327251.6:n.1704+129G=
ENST00000621962.1:c.1587+129G=	ENSP00000482291.1:n.1587+129G=
NM_000625.4:c.1704+129G= MANE Select	NP_000616.3:n.1704+129G=
XM_011524859.1:c.1704+129G=	XP_011523161.1:n.1704+129G=
XM_011524860.1:c.1701+129G=	XP_011523162.1:n.1701+129G=
XM_011524861.1:c.1704+129G=	XP_011523163.1:n.1704+129G=
XM_011524862.1:c.1038+129G=	XP_011523164.1:n.1038+129G=