Canonical Allele Identifier: CA498759281

Gene: NOS2

Linked Data

• dbSNP Id: rs1060822
• MyVariant Identifiers: chr17:g.26092631A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27765605A>T , CM000679.2:g.27765605A>T	GRCh38
NC_000017.10:g.26092631A>T , CM000679.1:g.26092631A>T	GRCh37
NC_000017.9:g.23116758A>T	NCBI36
NG_011470.1:g.39925T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*3092+2T>A	ENSP00000513259.1:n.*3092+2T>A
ENST00000697338.1:c.2206T>A	ENSP00000513260.1:n.2206T>A
ENST00000697339.1:c.1390+2T>A	ENSP00000513261.1:n.1390+2T>A
ENST00000697340.1:c.*1075T>A	ENSP00000513262.1:n.*1075T>A
ENST00000697341.1:n.2328T>A
ENST00000313735.11:c.2358T>A MANE Select	ENSP00000327251.6:p.Gly786=
ENST00000646938.1:c.2355T>A	ENSP00000494870.1:p.Gly785=
ENST00000313735.10:c.2358T>A	ENSP00000327251.6:p.Gly786=
ENST00000621962.1:c.2241T>A	ENSP00000482291.1:p.Gly747=
NM_000625.4:c.2358T>A MANE Select	NP_000616.3:p.Gly786=
XM_011524859.1:c.2358T>A	XP_011523161.1:p.Gly786=
XM_011524860.1:c.2355T>A	XP_011523162.1:p.Gly785=
XM_011524861.1:c.2356+2T>A	XP_011523163.1:n.2356+2T>A
XM_011524862.1:c.1692T>A	XP_011523164.1:p.Gly564=