Canonical Allele Identifier: CA289063554

Gene: NOS2

Linked Data

• dbSNP Id: rs764392596
• gnomAD v3: 17-27783599-C-T
• gnomAD v4: 17-27783599-C-T
• MyVariant Identifiers: chr17:g.26110625C>T (hg19) ; chr17:g.27783599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783599C>T , CM000679.2:g.27783599C>T	GRCh38
NC_000017.10:g.26110625C>T , CM000679.1:g.26110625C>T	GRCh37
NC_000017.9:g.23134752C>T	NCBI36
NG_011470.1:g.21931G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.319-493G>A	ENSP00000513259.1:n.319-493G>A
ENST00000697338.1:c.316-493G>A	ENSP00000513260.1:n.316-493G>A
ENST00000697339.1:c.315+5210G>A	ENSP00000513261.1:n.315+5210G>A
ENST00000697340.1:c.465-493G>A	ENSP00000513262.1:n.465-493G>A
ENST00000697341.1:n.438-493G>A
ENST00000313735.11:c.468-493G>A MANE Select	ENSP00000327251.6:n.468-493G>A
ENST00000646938.1:c.465-493G>A	ENSP00000494870.1:n.465-493G>A
ENST00000313735.10:c.468-493G>A	ENSP00000327251.6:n.468-493G>A
ENST00000621962.1:c.468-493G>A	ENSP00000482291.1:n.468-493G>A
NM_000625.4:c.468-493G>A MANE Select	NP_000616.3:n.468-493G>A
XM_011524859.1:c.468-493G>A	XP_011523161.1:n.468-493G>A
XM_011524860.1:c.465-493G>A	XP_011523162.1:n.465-493G>A
XM_011524861.1:c.468-493G>A	XP_011523163.1:n.468-493G>A
XM_011524862.1:c.-199-493G>A	XP_011523164.1:n.-199-493G>A