Canonical Allele Identifier: CA498770821

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26109106A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782080A>C , CM000679.2:g.27782080A>C	GRCh38
NC_000017.10:g.26109106A>C , CM000679.1:g.26109106A>C	GRCh37
NC_000017.9:g.23133233A>C	NCBI36
NG_011470.1:g.23450T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*103T>G	ENSP00000513259.1:n.*103T>G
ENST00000697338.1:c.505T>G	ENSP00000513260.1:n.505T>G
ENST00000697339.1:c.315+6729T>G	ENSP00000513261.1:n.315+6729T>G
ENST00000697340.1:c.654T>G	ENSP00000513262.1:p.Thr218=
ENST00000697341.1:n.627T>G
ENST00000313735.11:c.657T>G MANE Select	ENSP00000327251.6:p.Thr219=
ENST00000646938.1:c.654T>G	ENSP00000494870.1:p.Thr218=
ENST00000313735.10:c.657T>G	ENSP00000327251.6:p.Thr219=
ENST00000621962.1:c.657T>G	ENSP00000482291.1:p.Thr219=
NM_000625.4:c.657T>G MANE Select	NP_000616.3:p.Thr219=
XM_011524859.1:c.657T>G	XP_011523161.1:p.Thr219=
XM_011524860.1:c.654T>G	XP_011523162.1:p.Thr218=
XM_011524861.1:c.657T>G	XP_011523163.1:p.Thr219=
XM_011524862.1:c.-10T>G	XP_011523164.1:n.-10T>G