Canonical Allele Identifier: CA2809097175

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27761813A>C , CM000679.2:g.27761813A>C	GRCh38
NC_000017.10:g.26088839A>C , CM000679.1:g.26088839A>C	GRCh37
NC_000017.9:g.23112966A>C	NCBI36
NG_011470.1:g.43717T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3465-582T>G	ENSP00000513259.1:n.*3465-582T>G
ENST00000697338.1:c.2649-582T>G	ENSP00000513260.1:n.2649-582T>G
ENST00000697339.1:c.1763-582T>G	ENSP00000513261.1:n.1763-582T>G
ENST00000697340.1:c.*1514-582T>G	ENSP00000513262.1:n.*1514-582T>G
ENST00000313735.11:c.2801-582T>G MANE Select	ENSP00000327251.6:n.2801-582T>G
ENST00000646938.1:c.2798-582T>G	ENSP00000494870.1:n.2798-582T>G
ENST00000313735.10:c.2801-582T>G	ENSP00000327251.6:n.2801-582T>G
ENST00000621962.1:c.2684-582T>G	ENSP00000482291.1:n.2684-582T>G
NM_000625.4:c.2801-582T>G MANE Select	NP_000616.3:n.2801-582T>G
XM_011524859.1:c.2801-582T>G	XP_011523161.1:n.2801-582T>G
XM_011524860.1:c.2798-582T>G	XP_011523162.1:n.2798-582T>G
XM_011524861.1:c.2729-582T>G	XP_011523163.1:n.2729-582T>G
XM_011524862.1:c.2135-582T>G	XP_011523164.1:n.2135-582T>G