Canonical Allele Identifier: CA398309074

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26109083A>G (hg19) ; chr17:g.27782057A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782057A>G , CM000679.2:g.27782057A>G	GRCh38
NC_000017.10:g.26109083A>G , CM000679.1:g.26109083A>G	GRCh37
NC_000017.9:g.23133210A>G	NCBI36
NG_011470.1:g.23473T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*126T>C	ENSP00000513259.1:n.*126T>C
ENST00000697338.1:c.528T>C	ENSP00000513260.1:n.528T>C
ENST00000697339.1:c.315+6752T>C	ENSP00000513261.1:n.315+6752T>C
ENST00000697340.1:c.677T>C	ENSP00000513262.1:p.Ile226Thr
ENST00000697341.1:n.650T>C
ENST00000313735.11:c.680T>C MANE Select	ENSP00000327251.6:p.Ile227Thr
ENST00000646938.1:c.677T>C	ENSP00000494870.1:p.Ile226Thr
ENST00000313735.10:c.680T>C	ENSP00000327251.6:p.Ile227Thr
ENST00000621962.1:c.680T>C	ENSP00000482291.1:p.Ile227Thr
NM_000625.4:c.680T>C MANE Select	NP_000616.3:p.Ile227Thr
XM_011524859.1:c.680T>C	XP_011523161.1:p.Ile227Thr
XM_011524860.1:c.677T>C	XP_011523162.1:p.Ile226Thr
XM_011524861.1:c.680T>C	XP_011523163.1:p.Ile227Thr
XM_011524862.1:c.14T>C	XP_011523164.1:p.Ile5Thr