Canonical Allele Identifier: CA398308938

Gene: NOS2

Linked Data

• gnomAD v4: 17-27782031-T-A
• MyVariant Identifiers: chr17:g.26109057T>A (hg19) ; chr17:g.27782031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782031T>A , CM000679.2:g.27782031T>A	GRCh38
NC_000017.10:g.26109057T>A , CM000679.1:g.26109057T>A	GRCh37
NC_000017.9:g.23133184T>A	NCBI36
NG_011470.1:g.23499A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*152A>T	ENSP00000513259.1:n.*152A>T
ENST00000697338.1:c.554A>T	ENSP00000513260.1:n.554A>T
ENST00000697339.1:c.315+6778A>T	ENSP00000513261.1:n.315+6778A>T
ENST00000697340.1:c.703A>T	ENSP00000513262.1:p.Asn235Tyr
ENST00000697341.1:n.676A>T
ENST00000313735.11:c.706A>T MANE Select	ENSP00000327251.6:p.Asn236Tyr
ENST00000646938.1:c.703A>T	ENSP00000494870.1:p.Asn235Tyr
ENST00000313735.10:c.706A>T	ENSP00000327251.6:p.Asn236Tyr
ENST00000621962.1:c.706A>T	ENSP00000482291.1:p.Asn236Tyr
NM_000625.4:c.706A>T MANE Select	NP_000616.3:p.Asn236Tyr
XM_011524859.1:c.706A>T	XP_011523161.1:p.Asn236Tyr
XM_011524860.1:c.703A>T	XP_011523162.1:p.Asn235Tyr
XM_011524861.1:c.706A>T	XP_011523163.1:p.Asn236Tyr
XM_011524862.1:c.40A>T	XP_011523164.1:p.Asn14Tyr