Canonical Allele Identifier: CA398301514

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096592A>C (hg19) ; chr17:g.27769566A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769566A>C , CM000679.2:g.27769566A>C	GRCh38
NC_000017.10:g.26096592A>C , CM000679.1:g.26096592A>C	GRCh37
NC_000017.9:g.23120719A>C	NCBI36
NG_011470.1:g.35964T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2564T>G	ENSP00000513259.1:n.*2564T>G
ENST00000697338.1:c.1676T>G	ENSP00000513260.1:n.1676T>G
ENST00000697339.1:c.862T>G	ENSP00000513261.1:p.Phe288Val
ENST00000697340.1:c.*545T>G	ENSP00000513262.1:n.*545T>G
ENST00000697341.1:n.1798T>G
ENST00000313735.11:c.1828T>G MANE Select	ENSP00000327251.6:p.Phe610Val
ENST00000646938.1:c.1825T>G	ENSP00000494870.1:p.Phe609Val
ENST00000313735.10:c.1828T>G	ENSP00000327251.6:p.Phe610Val
ENST00000621962.1:c.1711T>G	ENSP00000482291.1:p.Phe571Val
NM_000625.4:c.1828T>G MANE Select	NP_000616.3:p.Phe610Val
XM_011524859.1:c.1828T>G	XP_011523161.1:p.Phe610Val
XM_011524860.1:c.1825T>G	XP_011523162.1:p.Phe609Val
XM_011524861.1:c.1828T>G	XP_011523163.1:p.Phe610Val
XM_011524862.1:c.1162T>G	XP_011523164.1:p.Phe388Val