Canonical Allele Identifier: CA982710893

Gene: NOS2

Linked Data

• dbSNP Id: rs1908922617
• gnomAD v3: 17-27783687-C-T
• gnomAD v4: 17-27783687-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783687C>T , CM000679.2:g.27783687C>T	GRCh38
NC_000017.10:g.26110713C>T , CM000679.1:g.26110713C>T	GRCh37
NC_000017.9:g.23134840C>T	NCBI36
NG_011470.1:g.21843G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.319-581G>A	ENSP00000513259.1:n.319-581G>A
ENST00000697338.1:c.316-581G>A	ENSP00000513260.1:n.316-581G>A
ENST00000697339.1:c.315+5122G>A	ENSP00000513261.1:n.315+5122G>A
ENST00000697340.1:c.465-581G>A	ENSP00000513262.1:n.465-581G>A
ENST00000697341.1:n.438-581G>A
ENST00000313735.11:c.468-581G>A MANE Select	ENSP00000327251.6:n.468-581G>A
ENST00000646938.1:c.465-581G>A	ENSP00000494870.1:n.465-581G>A
ENST00000313735.10:c.468-581G>A	ENSP00000327251.6:n.468-581G>A
ENST00000621962.1:c.468-581G>A	ENSP00000482291.1:n.468-581G>A
NM_000625.4:c.468-581G>A MANE Select	NP_000616.3:n.468-581G>A
XM_011524859.1:c.468-581G>A	XP_011523161.1:n.468-581G>A
XM_011524860.1:c.465-581G>A	XP_011523162.1:n.465-581G>A
XM_011524861.1:c.468-581G>A	XP_011523163.1:n.468-581G>A
XM_011524862.1:c.-199-581G>A	XP_011523164.1:n.-199-581G>A