Canonical Allele Identifier: CA498770671

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26109058G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782032G>T , CM000679.2:g.27782032G>T	GRCh38
NC_000017.10:g.26109058G>T , CM000679.1:g.26109058G>T	GRCh37
NC_000017.9:g.23133185G>T	NCBI36
NG_011470.1:g.23498C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*151C>A	ENSP00000513259.1:n.*151C>A
ENST00000697338.1:c.553C>A	ENSP00000513260.1:n.553C>A
ENST00000697339.1:c.315+6777C>A	ENSP00000513261.1:n.315+6777C>A
ENST00000697340.1:c.702C>A	ENSP00000513262.1:p.Thr234=
ENST00000697341.1:n.675C>A
ENST00000313735.11:c.705C>A MANE Select	ENSP00000327251.6:p.Thr235=
ENST00000646938.1:c.702C>A	ENSP00000494870.1:p.Thr234=
ENST00000313735.10:c.705C>A	ENSP00000327251.6:p.Thr235=
ENST00000621962.1:c.705C>A	ENSP00000482291.1:p.Thr235=
NM_000625.4:c.705C>A MANE Select	NP_000616.3:p.Thr235=
XM_011524859.1:c.705C>A	XP_011523161.1:p.Thr235=
XM_011524860.1:c.702C>A	XP_011523162.1:p.Thr234=
XM_011524861.1:c.705C>A	XP_011523163.1:p.Thr235=
XM_011524862.1:c.39C>A	XP_011523164.1:p.Thr13=