Canonical Allele Identifier: CA498770644

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26109049G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782023G>A , CM000679.2:g.27782023G>A	GRCh38
NC_000017.10:g.26109049G>A , CM000679.1:g.26109049G>A	GRCh37
NC_000017.9:g.23133176G>A	NCBI36
NG_011470.1:g.23507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*160C>T	ENSP00000513259.1:n.*160C>T
ENST00000697338.1:c.562C>T	ENSP00000513260.1:n.562C>T
ENST00000697339.1:c.315+6786C>T	ENSP00000513261.1:n.315+6786C>T
ENST00000697340.1:c.711C>T	ENSP00000513262.1:p.Gly237=
ENST00000697341.1:n.684C>T
ENST00000313735.11:c.714C>T MANE Select	ENSP00000327251.6:p.Gly238=
ENST00000646938.1:c.711C>T	ENSP00000494870.1:p.Gly237=
ENST00000313735.10:c.714C>T	ENSP00000327251.6:p.Gly238=
ENST00000621962.1:c.714C>T	ENSP00000482291.1:p.Gly238=
NM_000625.4:c.714C>T MANE Select	NP_000616.3:p.Gly238=
XM_011524859.1:c.714C>T	XP_011523161.1:p.Gly238=
XM_011524860.1:c.711C>T	XP_011523162.1:p.Gly237=
XM_011524861.1:c.714C>T	XP_011523163.1:p.Gly238=
XM_011524862.1:c.48C>T	XP_011523164.1:p.Gly16=