Canonical Allele Identifier: CA498759229

Gene: NOS2

Linked Data

• dbSNP Id: rs746034121
• gnomAD v2: 17-26092565-C-T
• gnomAD v4: 17-27765539-C-T
• MyVariant Identifiers: chr17:g.26092565C>T (hg19) ; chr17:g.27765539C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27765539C>T , CM000679.2:g.27765539C>T	GRCh38
NC_000017.10:g.26092565C>T , CM000679.1:g.26092565C>T	GRCh37
NC_000017.9:g.23116692C>T	NCBI36
NG_011470.1:g.39991G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*3092+68G>A	ENSP00000513259.1:n.*3092+68G>A
ENST00000697338.1:c.2272G>A	ENSP00000513260.1:n.2272G>A
ENST00000697339.1:c.1390+68G>A	ENSP00000513261.1:n.1390+68G>A
ENST00000697340.1:c.*1141G>A	ENSP00000513262.1:n.*1141G>A
ENST00000697341.1:n.2394G>A
ENST00000313735.11:c.2424G>A MANE Select	ENSP00000327251.6:p.Glu808=
ENST00000646938.1:c.2421G>A	ENSP00000494870.1:p.Glu807=
ENST00000313735.10:c.2424G>A	ENSP00000327251.6:p.Glu808=
ENST00000621962.1:c.2307G>A	ENSP00000482291.1:p.Glu769=
NM_000625.4:c.2424G>A MANE Select	NP_000616.3:p.Glu808=
XM_011524859.1:c.2424G>A	XP_011523161.1:p.Glu808=
XM_011524860.1:c.2421G>A	XP_011523162.1:p.Glu807=
XM_011524861.1:c.2356+68G>A	XP_011523163.1:n.2356+68G>A
XM_011524862.1:c.1758G>A	XP_011523164.1:p.Glu586=