Canonical Allele Identifier: CA2254013120

Gene: NOS2

Linked Data

• dbSNP Id: rs1908777170

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27779554T>C , CM000679.2:g.27779554T>C	GRCh38
NC_000017.10:g.26106580T>C , CM000679.1:g.26106580T>C	GRCh37
NC_000017.9:g.23130707T>C	NCBI36
NG_011470.1:g.25976A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*451-498A>G	ENSP00000513259.1:n.*451-498A>G
ENST00000697338.1:c.853-498A>G	ENSP00000513260.1:n.853-498A>G
ENST00000697339.1:c.316-5103A>G	ENSP00000513261.1:n.316-5103A>G
ENST00000697340.1:c.1002-498A>G	ENSP00000513262.1:n.1002-498A>G
ENST00000697341.1:n.975-498A>G
ENST00000313735.11:c.1005-498A>G MANE Select	ENSP00000327251.6:n.1005-498A>G
ENST00000646938.1:c.1002-498A>G	ENSP00000494870.1:n.1002-498A>G
ENST00000313735.10:c.1005-498A>G	ENSP00000327251.6:n.1005-498A>G
ENST00000621962.1:c.888-498A>G	ENSP00000482291.1:n.888-498A>G
NM_000625.4:c.1005-498A>G MANE Select	NP_000616.3:n.1005-498A>G
XM_011524859.1:c.1005-498A>G	XP_011523161.1:n.1005-498A>G
XM_011524860.1:c.1002-498A>G	XP_011523162.1:n.1002-498A>G
XM_011524861.1:c.1005-498A>G	XP_011523163.1:n.1005-498A>G
XM_011524862.1:c.339-498A>G	XP_011523164.1:n.339-498A>G