Canonical Allele Identifier: CA2254014854

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783783C= , CM000679.2:g.27783783C=	GRCh38
NC_000017.10:g.26110809C= , CM000679.1:g.26110809C=	GRCh37
NC_000017.9:g.23134936C=	NCBI36
NG_011470.1:g.21747G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.319-677G=	ENSP00000513259.1:n.319-677G=
ENST00000697338.1:c.316-677G=	ENSP00000513260.1:n.316-677G=
ENST00000697339.1:c.315+5026G=	ENSP00000513261.1:n.315+5026G=
ENST00000697340.1:c.465-677G=	ENSP00000513262.1:n.465-677G=
ENST00000697341.1:n.438-677G=
ENST00000313735.11:c.468-677G= MANE Select	ENSP00000327251.6:n.468-677G=
ENST00000646938.1:c.465-677G=	ENSP00000494870.1:n.465-677G=
ENST00000313735.10:c.468-677G=	ENSP00000327251.6:n.468-677G=
ENST00000621962.1:c.468-677G=	ENSP00000482291.1:n.468-677G=
NM_000625.4:c.468-677G= MANE Select	NP_000616.3:n.468-677G=
XM_011524859.1:c.468-677G=	XP_011523161.1:n.468-677G=
XM_011524860.1:c.465-677G=	XP_011523162.1:n.465-677G=
XM_011524861.1:c.468-677G=	XP_011523163.1:n.468-677G=
XM_011524862.1:c.-199-677G=	XP_011523164.1:n.-199-677G=