Canonical Allele Identifier: CA398301372

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096566T>A (hg19) ; chr17:g.27769540T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769540T>A , CM000679.2:g.27769540T>A	GRCh38
NC_000017.10:g.26096566T>A , CM000679.1:g.26096566T>A	GRCh37
NC_000017.9:g.23120693T>A	NCBI36
NG_011470.1:g.35990A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2590A>T	ENSP00000513259.1:n.*2590A>T
ENST00000697338.1:c.1702A>T	ENSP00000513260.1:n.1702A>T
ENST00000697339.1:c.888A>T	ENSP00000513261.1:p.Lys296Asn
ENST00000697340.1:c.*571A>T	ENSP00000513262.1:n.*571A>T
ENST00000697341.1:n.1824A>T
ENST00000313735.11:c.1854A>T MANE Select	ENSP00000327251.6:p.Lys618Asn
ENST00000646938.1:c.1851A>T	ENSP00000494870.1:p.Lys617Asn
ENST00000313735.10:c.1854A>T	ENSP00000327251.6:p.Lys618Asn
ENST00000621962.1:c.1737A>T	ENSP00000482291.1:p.Lys579Asn
NM_000625.4:c.1854A>T MANE Select	NP_000616.3:p.Lys618Asn
XM_011524859.1:c.1854A>T	XP_011523161.1:p.Lys618Asn
XM_011524860.1:c.1851A>T	XP_011523162.1:p.Lys617Asn
XM_011524861.1:c.1854A>T	XP_011523163.1:p.Lys618Asn
XM_011524862.1:c.1188A>T	XP_011523164.1:p.Lys396Asn