Canonical Allele Identifier: CA398298459

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26092564T>G (hg19) ; chr17:g.27765538T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27765538T>G , CM000679.2:g.27765538T>G	GRCh38
NC_000017.10:g.26092564T>G , CM000679.1:g.26092564T>G	GRCh37
NC_000017.9:g.23116691T>G	NCBI36
NG_011470.1:g.39992A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3092+69A>C	ENSP00000513259.1:n.*3092+69A>C
ENST00000697338.1:c.2273A>C	ENSP00000513260.1:n.2273A>C
ENST00000697339.1:c.1390+69A>C	ENSP00000513261.1:n.1390+69A>C
ENST00000697340.1:c.*1142A>C	ENSP00000513262.1:n.*1142A>C
ENST00000697341.1:n.2395A>C
ENST00000313735.11:c.2425A>C MANE Select	ENSP00000327251.6:p.Ser809Arg
ENST00000646938.1:c.2422A>C	ENSP00000494870.1:p.Ser808Arg
ENST00000313735.10:c.2425A>C	ENSP00000327251.6:p.Ser809Arg
ENST00000621962.1:c.2308A>C	ENSP00000482291.1:p.Ser770Arg
NM_000625.4:c.2425A>C MANE Select	NP_000616.3:p.Ser809Arg
XM_011524859.1:c.2425A>C	XP_011523161.1:p.Ser809Arg
XM_011524860.1:c.2422A>C	XP_011523162.1:p.Ser808Arg
XM_011524861.1:c.2356+69A>C	XP_011523163.1:n.2356+69A>C
XM_011524862.1:c.1759A>C	XP_011523164.1:p.Ser587Arg