Canonical Allele Identifier: CA727707388

Gene: NOS2

Linked Data

• dbSNP Id: rs1189277093
• gnomAD v3: 17-27769593-A-T
• gnomAD v4: 17-27769593-A-T
• MyVariant Identifiers: chr17:g.26096619A>T (hg19) ; chr17:g.27769593A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769593A>T , CM000679.2:g.27769593A>T	GRCh38
NC_000017.10:g.26096619A>T , CM000679.1:g.26096619A>T	GRCh37
NC_000017.9:g.23120746A>T	NCBI36
NG_011470.1:g.35937T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2546-9T>A	ENSP00000513259.1:n.*2546-9T>A
ENST00000697338.1:c.1658-9T>A	ENSP00000513260.1:n.1658-9T>A
ENST00000697339.1:c.844-9T>A	ENSP00000513261.1:n.844-9T>A
ENST00000697340.1:c.*527-9T>A	ENSP00000513262.1:n.*527-9T>A
ENST00000697341.1:n.1780-9T>A
ENST00000313735.11:c.1810-9T>A MANE Select	ENSP00000327251.6:n.1810-9T>A
ENST00000646938.1:c.1807-9T>A	ENSP00000494870.1:n.1807-9T>A
ENST00000313735.10:c.1810-9T>A	ENSP00000327251.6:n.1810-9T>A
ENST00000621962.1:c.1693-9T>A	ENSP00000482291.1:n.1693-9T>A
NM_000625.4:c.1810-9T>A MANE Select	NP_000616.3:n.1810-9T>A
XM_011524859.1:c.1810-9T>A	XP_011523161.1:n.1810-9T>A
XM_011524860.1:c.1807-9T>A	XP_011523162.1:n.1807-9T>A
XM_011524861.1:c.1810-9T>A	XP_011523163.1:n.1810-9T>A
XM_011524862.1:c.1144-9T>A	XP_011523164.1:n.1144-9T>A