Canonical Allele Identifier: CA498760880

Gene: NOS2

Linked Data

• dbSNP Id: rs1217512050
• MyVariant Identifiers: chr17:g.26096593G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769567G>C , CM000679.2:g.27769567G>C	GRCh38
NC_000017.10:g.26096593G>C , CM000679.1:g.26096593G>C	GRCh37
NC_000017.9:g.23120720G>C	NCBI36
NG_011470.1:g.35963C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2563C>G	ENSP00000513259.1:n.*2563C>G
ENST00000697338.1:c.1675C>G	ENSP00000513260.1:n.1675C>G
ENST00000697339.1:c.861C>G	ENSP00000513261.1:p.Leu287=
ENST00000697340.1:c.*544C>G	ENSP00000513262.1:n.*544C>G
ENST00000697341.1:n.1797C>G
ENST00000313735.11:c.1827C>G MANE Select	ENSP00000327251.6:p.Leu609=
ENST00000646938.1:c.1824C>G	ENSP00000494870.1:p.Leu608=
ENST00000313735.10:c.1827C>G	ENSP00000327251.6:p.Leu609=
ENST00000621962.1:c.1710C>G	ENSP00000482291.1:p.Leu570=
NM_000625.4:c.1827C>G MANE Select	NP_000616.3:p.Leu609=
XM_011524859.1:c.1827C>G	XP_011523161.1:p.Leu609=
XM_011524860.1:c.1824C>G	XP_011523162.1:p.Leu608=
XM_011524861.1:c.1827C>G	XP_011523163.1:p.Leu609=
XM_011524862.1:c.1161C>G	XP_011523164.1:p.Leu387=