Canonical Allele Identifier: CA2254003027

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27757521C= , CM000679.2:g.27757521C=	GRCh38
NC_000017.10:g.26084547C= , CM000679.1:g.26084547C=	GRCh37
NC_000017.9:g.23108674C=	NCBI36
NG_011470.1:g.48009G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*4019-168G=	ENSP00000513259.1:n.*4019-168G=
ENST00000697338.1:c.3203-168G=	ENSP00000513260.1:n.3203-168G=
ENST00000697339.1:c.2317-168G=	ENSP00000513261.1:n.2317-168G=
ENST00000697340.1:c.*2068-168G=	ENSP00000513262.1:n.*2068-168G=
ENST00000313735.11:c.3355-168G= MANE Select	ENSP00000327251.6:n.3355-168G=
ENST00000646938.1:c.3352-168G=	ENSP00000494870.1:n.3352-168G=
ENST00000313735.10:c.3355-168G=	ENSP00000327251.6:n.3355-168G=
ENST00000621962.1:c.3238-168G=	ENSP00000482291.1:n.3238-168G=
NM_000625.4:c.3355-168G= MANE Select	NP_000616.3:n.3355-168G=
XM_011524859.1:c.3355-168G=	XP_011523161.1:n.3355-168G=
XM_011524860.1:c.3352-168G=	XP_011523162.1:n.3352-168G=
XM_011524861.1:c.3283-168G=	XP_011523163.1:n.3283-168G=
XM_011524862.1:c.2689-168G=	XP_011523164.1:n.2689-168G=