Canonical Allele Identifier: CA398308920

Gene: NOS2

Linked Data

• dbSNP Id: rs1252742586
• gnomAD v2: 17-26109054-T-C
• MyVariant Identifiers: chr17:g.26109054T>C (hg19) ; chr17:g.27782028T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782028T>C , CM000679.2:g.27782028T>C	GRCh38
NC_000017.10:g.26109054T>C , CM000679.1:g.26109054T>C	GRCh37
NC_000017.9:g.23133181T>C	NCBI36
NG_011470.1:g.23502A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*155A>G	ENSP00000513259.1:n.*155A>G
ENST00000697338.1:c.557A>G	ENSP00000513260.1:n.557A>G
ENST00000697339.1:c.315+6781A>G	ENSP00000513261.1:n.315+6781A>G
ENST00000697340.1:c.706A>G	ENSP00000513262.1:p.Asn236Asp
ENST00000697341.1:n.679A>G
ENST00000313735.11:c.709A>G MANE Select	ENSP00000327251.6:p.Asn237Asp
ENST00000646938.1:c.706A>G	ENSP00000494870.1:p.Asn236Asp
ENST00000313735.10:c.709A>G	ENSP00000327251.6:p.Asn237Asp
ENST00000621962.1:c.709A>G	ENSP00000482291.1:p.Asn237Asp
NM_000625.4:c.709A>G MANE Select	NP_000616.3:p.Asn237Asp
XM_011524859.1:c.709A>G	XP_011523161.1:p.Asn237Asp
XM_011524860.1:c.706A>G	XP_011523162.1:p.Asn236Asp
XM_011524861.1:c.709A>G	XP_011523163.1:p.Asn237Asp
XM_011524862.1:c.43A>G	XP_011523164.1:p.Asn15Asp