Canonical Allele Identifier: CA289062181

Gene: NOS2

Linked Data

• dbSNP Id: rs966635064
• gnomAD v3: 17-27782335-G-C
• gnomAD v4: 17-27782335-G-C
• MyVariant Identifiers: chr17:g.26109361G>C (hg19) ; chr17:g.27782335G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782335G>C , CM000679.2:g.27782335G>C	GRCh38
NC_000017.10:g.26109361G>C , CM000679.1:g.26109361G>C	GRCh37
NC_000017.9:g.23133488G>C	NCBI36
NG_011470.1:g.23195C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*77-229C>G	ENSP00000513259.1:n.*77-229C>G
ENST00000697338.1:c.479-229C>G	ENSP00000513260.1:n.479-229C>G
ENST00000697339.1:c.315+6474C>G	ENSP00000513261.1:n.315+6474C>G
ENST00000697340.1:c.628-229C>G	ENSP00000513262.1:n.628-229C>G
ENST00000697341.1:n.601-229C>G
ENST00000313735.11:c.631-229C>G MANE Select	ENSP00000327251.6:n.631-229C>G
ENST00000646938.1:c.628-229C>G	ENSP00000494870.1:n.628-229C>G
ENST00000313735.10:c.631-229C>G	ENSP00000327251.6:n.631-229C>G
ENST00000621962.1:c.631-229C>G	ENSP00000482291.1:n.631-229C>G
NM_000625.4:c.631-229C>G MANE Select	NP_000616.3:n.631-229C>G
XM_011524859.1:c.631-229C>G	XP_011523161.1:n.631-229C>G
XM_011524860.1:c.628-229C>G	XP_011523162.1:n.628-229C>G
XM_011524861.1:c.631-229C>G	XP_011523163.1:n.631-229C>G
XM_011524862.1:c.-36-229C>G	XP_011523164.1:n.-36-229C>G