Canonical Allele Identifier: CA398301392

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096570T>C (hg19) ; chr17:g.27769544T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769544T>C , CM000679.2:g.27769544T>C	GRCh38
NC_000017.10:g.26096570T>C , CM000679.1:g.26096570T>C	GRCh37
NC_000017.9:g.23120697T>C	NCBI36
NG_011470.1:g.35986A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2586A>G	ENSP00000513259.1:n.*2586A>G
ENST00000697338.1:c.1698A>G	ENSP00000513260.1:n.1698A>G
ENST00000697339.1:c.884A>G	ENSP00000513261.1:p.Asn295Ser
ENST00000697340.1:c.*567A>G	ENSP00000513262.1:n.*567A>G
ENST00000697341.1:n.1820A>G
ENST00000313735.11:c.1850A>G MANE Select	ENSP00000327251.6:p.Asn617Ser
ENST00000646938.1:c.1847A>G	ENSP00000494870.1:p.Asn616Ser
ENST00000313735.10:c.1850A>G	ENSP00000327251.6:p.Asn617Ser
ENST00000621962.1:c.1733A>G	ENSP00000482291.1:p.Asn578Ser
NM_000625.4:c.1850A>G MANE Select	NP_000616.3:p.Asn617Ser
XM_011524859.1:c.1850A>G	XP_011523161.1:p.Asn617Ser
XM_011524860.1:c.1847A>G	XP_011523162.1:p.Asn616Ser
XM_011524861.1:c.1850A>G	XP_011523163.1:p.Asn617Ser
XM_011524862.1:c.1184A>G	XP_011523164.1:p.Asn395Ser