Canonical Allele Identifier: CA498760846

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096584C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769558C>A , CM000679.2:g.27769558C>A	GRCh38
NC_000017.10:g.26096584C>A , CM000679.1:g.26096584C>A	GRCh37
NC_000017.9:g.23120711C>A	NCBI36
NG_011470.1:g.35972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2572G>T	ENSP00000513259.1:n.*2572G>T
ENST00000697338.1:c.1684G>T	ENSP00000513260.1:n.1684G>T
ENST00000697339.1:c.870G>T	ENSP00000513261.1:p.Leu290=
ENST00000697340.1:c.*553G>T	ENSP00000513262.1:n.*553G>T
ENST00000697341.1:n.1806G>T
ENST00000313735.11:c.1836G>T MANE Select	ENSP00000327251.6:p.Leu612=
ENST00000646938.1:c.1833G>T	ENSP00000494870.1:p.Leu611=
ENST00000313735.10:c.1836G>T	ENSP00000327251.6:p.Leu612=
ENST00000621962.1:c.1719G>T	ENSP00000482291.1:p.Leu573=
NM_000625.4:c.1836G>T MANE Select	NP_000616.3:p.Leu612=
XM_011524859.1:c.1836G>T	XP_011523161.1:p.Leu612=
XM_011524860.1:c.1833G>T	XP_011523162.1:p.Leu611=
XM_011524861.1:c.1836G>T	XP_011523163.1:p.Leu612=
XM_011524862.1:c.1170G>T	XP_011523164.1:p.Leu390=