Canonical Allele Identifier: CA398308827

Gene: NOS2

Linked Data

• dbSNP Id: rs2142518008
• MyVariant Identifiers: chr17:g.26109039A>C (hg19) ; chr17:g.27782013A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782013A>C , CM000679.2:g.27782013A>C	GRCh38
NC_000017.10:g.26109039A>C , CM000679.1:g.26109039A>C	GRCh37
NC_000017.9:g.23133166A>C	NCBI36
NG_011470.1:g.23517T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*168+2T>G	ENSP00000513259.1:n.*168+2T>G
ENST00000697338.1:c.570+2T>G	ENSP00000513260.1:n.570+2T>G
ENST00000697339.1:c.315+6796T>G	ENSP00000513261.1:n.315+6796T>G
ENST00000697340.1:c.719+2T>G	ENSP00000513262.1:n.719+2T>G
ENST00000697341.1:n.692+2T>G
ENST00000313735.11:c.722+2T>G MANE Select	ENSP00000327251.6:n.722+2T>G
ENST00000646938.1:c.719+2T>G	ENSP00000494870.1:n.719+2T>G
ENST00000313735.10:c.722+2T>G	ENSP00000327251.6:n.722+2T>G
ENST00000621962.1:c.722+2T>G	ENSP00000482291.1:n.722+2T>G
NM_000625.4:c.722+2T>G MANE Select	NP_000616.3:n.722+2T>G
XM_011524859.1:c.722+2T>G	XP_011523161.1:n.722+2T>G
XM_011524860.1:c.719+2T>G	XP_011523162.1:n.719+2T>G
XM_011524861.1:c.722+2T>G	XP_011523163.1:n.722+2T>G
XM_011524862.1:c.56+2T>G	XP_011523164.1:n.56+2T>G