Canonical Allele Identifier: CA398301543

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096598A>T (hg19) ; chr17:g.27769572A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769572A>T , CM000679.2:g.27769572A>T	GRCh38
NC_000017.10:g.26096598A>T , CM000679.1:g.26096598A>T	GRCh37
NC_000017.9:g.23120725A>T	NCBI36
NG_011470.1:g.35958T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2558T>A	ENSP00000513259.1:n.*2558T>A
ENST00000697338.1:c.1670T>A	ENSP00000513260.1:n.1670T>A
ENST00000697339.1:c.856T>A	ENSP00000513261.1:p.Ser286Thr
ENST00000697340.1:c.*539T>A	ENSP00000513262.1:n.*539T>A
ENST00000697341.1:n.1792T>A
ENST00000313735.11:c.1822T>A MANE Select	ENSP00000327251.6:p.Ser608Thr
ENST00000646938.1:c.1819T>A	ENSP00000494870.1:p.Ser607Thr
ENST00000313735.10:c.1822T>A	ENSP00000327251.6:p.Ser608Thr
ENST00000621962.1:c.1705T>A	ENSP00000482291.1:p.Ser569Thr
NM_000625.4:c.1822T>A MANE Select	NP_000616.3:p.Ser608Thr
XM_011524859.1:c.1822T>A	XP_011523161.1:p.Ser608Thr
XM_011524860.1:c.1819T>A	XP_011523162.1:p.Ser607Thr
XM_011524861.1:c.1822T>A	XP_011523163.1:p.Ser608Thr
XM_011524862.1:c.1156T>A	XP_011523164.1:p.Ser386Thr