Canonical Allele Identifier: CA727709807

Gene: NOS2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27773295A>C , CM000679.2:g.27773295A>C	GRCh38
NC_000017.10:g.26100321A>C , CM000679.1:g.26100321A>C	GRCh37
NC_000017.9:g.23124448A>C	NCBI36
NG_011470.1:g.32235T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*923-52T>G	ENSP00000513259.1:n.*923-52T>G
ENST00000697338.1:c.1325-52T>G	ENSP00000513260.1:n.1325-52T>G
ENST00000697339.1:c.511-52T>G	ENSP00000513261.1:n.511-52T>G
ENST00000697340.1:c.*194-52T>G	ENSP00000513262.1:n.*194-52T>G
ENST00000697341.1:n.1447-52T>G
ENST00000313735.11:c.1477-52T>G MANE Select	ENSP00000327251.6:n.1477-52T>G
ENST00000646938.1:c.1474-52T>G	ENSP00000494870.1:n.1474-52T>G
ENST00000313735.10:c.1477-52T>G	ENSP00000327251.6:n.1477-52T>G
ENST00000621962.1:c.1360-52T>G	ENSP00000482291.1:n.1360-52T>G
NM_000625.4:c.1477-52T>G MANE Select	NP_000616.3:n.1477-52T>G
XM_011524859.1:c.1477-52T>G	XP_011523161.1:n.1477-52T>G
XM_011524860.1:c.1474-52T>G	XP_011523162.1:n.1474-52T>G
XM_011524861.1:c.1477-52T>G	XP_011523163.1:n.1477-52T>G
XM_011524862.1:c.811-52T>G	XP_011523164.1:n.811-52T>G