Canonical Allele Identifier: CA289062137

Gene: NOS2

Linked Data

• dbSNP Id: rs184785164
• gnomAD v3: 17-27782259-C-G
• gnomAD v4: 17-27782259-C-G
• MyVariant Identifiers: chr17:g.26109285C>G (hg19) ; chr17:g.27782259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782259C>G , CM000679.2:g.27782259C>G	GRCh38
NC_000017.10:g.26109285C>G , CM000679.1:g.26109285C>G	GRCh37
NC_000017.9:g.23133412C>G	NCBI36
NG_011470.1:g.23271G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*77-153G>C	ENSP00000513259.1:n.*77-153G>C
ENST00000697338.1:c.479-153G>C	ENSP00000513260.1:n.479-153G>C
ENST00000697339.1:c.315+6550G>C	ENSP00000513261.1:n.315+6550G>C
ENST00000697340.1:c.628-153G>C	ENSP00000513262.1:n.628-153G>C
ENST00000697341.1:n.601-153G>C
ENST00000313735.11:c.631-153G>C MANE Select	ENSP00000327251.6:n.631-153G>C
ENST00000646938.1:c.628-153G>C	ENSP00000494870.1:n.628-153G>C
ENST00000313735.10:c.631-153G>C	ENSP00000327251.6:n.631-153G>C
ENST00000621962.1:c.631-153G>C	ENSP00000482291.1:n.631-153G>C
NM_000625.4:c.631-153G>C MANE Select	NP_000616.3:n.631-153G>C
XM_011524859.1:c.631-153G>C	XP_011523161.1:n.631-153G>C
XM_011524860.1:c.628-153G>C	XP_011523162.1:n.628-153G>C
XM_011524861.1:c.631-153G>C	XP_011523163.1:n.631-153G>C
XM_011524862.1:c.-36-153G>C	XP_011523164.1:n.-36-153G>C