Canonical Allele Identifier: CA2581299636

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27761829G>C , CM000679.2:g.27761829G>C	GRCh38
NC_000017.10:g.26088855G>C , CM000679.1:g.26088855G>C	GRCh37
NC_000017.9:g.23112982G>C	NCBI36
NG_011470.1:g.43701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3465-598C>G	ENSP00000513259.1:n.*3465-598C>G
ENST00000697338.1:c.2649-598C>G	ENSP00000513260.1:n.2649-598C>G
ENST00000697339.1:c.1763-598C>G	ENSP00000513261.1:n.1763-598C>G
ENST00000697340.1:c.*1514-598C>G	ENSP00000513262.1:n.*1514-598C>G
ENST00000313735.11:c.2801-598C>G MANE Select	ENSP00000327251.6:n.2801-598C>G
ENST00000646938.1:c.2798-598C>G	ENSP00000494870.1:n.2798-598C>G
ENST00000313735.10:c.2801-598C>G	ENSP00000327251.6:n.2801-598C>G
ENST00000621962.1:c.2684-598C>G	ENSP00000482291.1:n.2684-598C>G
NM_000625.4:c.2801-598C>G MANE Select	NP_000616.3:n.2801-598C>G
XM_011524859.1:c.2801-598C>G	XP_011523161.1:n.2801-598C>G
XM_011524860.1:c.2798-598C>G	XP_011523162.1:n.2798-598C>G
XM_011524861.1:c.2729-598C>G	XP_011523163.1:n.2729-598C>G
XM_011524862.1:c.2135-598C>G	XP_011523164.1:n.2135-598C>G