Canonical Allele Identifier: CA2254013727

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27781014T= , CM000679.2:g.27781014T=	GRCh38
NC_000017.10:g.26108040T= , CM000679.1:g.26108040T=	GRCh37
NC_000017.9:g.23132167T=	NCBI36
NG_011470.1:g.24516A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000625.4:c.864+22A= MANE Select	NP_000616.3:n.864+22A=
ENST00000313735.11:c.864+22A= MANE Select	ENSP00000327251.6:n.864+22A=
ENST00000313735.10:c.864+22A=	ENSP00000327251.6:n.864+22A=
ENST00000621962.1:c.789+97A=	ENSP00000482291.1:n.789+97A=
ENST00000646938.1:c.861+22A=	ENSP00000494870.1:n.861+22A=
ENST00000697337.1:c.*310+22A=	ENSP00000513259.1:n.*310+22A=
ENST00000697338.1:c.712+22A=	ENSP00000513260.1:n.712+22A=
ENST00000697339.1:c.316-6563A=	ENSP00000513261.1:n.316-6563A=
ENST00000697340.1:c.861+22A=	ENSP00000513262.1:n.861+22A=
ENST00000697341.1:n.834+22A=
XM_011524859.1:c.864+22A=	XP_011523161.1:n.864+22A=
XM_011524860.1:c.861+22A=	XP_011523162.1:n.861+22A=
XM_011524861.1:c.864+22A=	XP_011523163.1:n.864+22A=
XM_011524862.1:c.198+22A=	XP_011523164.1:n.198+22A=