Canonical Allele Identifier: CA2254020890

Gene: NOS2

Linked Data

• dbSNP Id: rs186436541

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27797636G>T , CM000679.2:g.27797636G>T	GRCh38
NC_000017.10:g.26124662G>T , CM000679.1:g.26124662G>T	GRCh37
NC_000017.9:g.23148789G>T	NCBI36
NG_011470.1:g.7894C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.110+1064C>A	ENSP00000513259.1:n.110+1064C>A
ENST00000313735.11:c.110+1064C>A MANE Select	ENSP00000327251.6:n.110+1064C>A
ENST00000313735.10:c.110+1064C>A	ENSP00000327251.6:n.110+1064C>A
ENST00000621962.1:c.110+1064C>A	ENSP00000482291.1:n.110+1064C>A
NM_000625.4:c.110+1064C>A MANE Select	NP_000616.3:n.110+1064C>A
XM_011524859.1:c.110+1064C>A	XP_011523161.1:n.110+1064C>A
XM_011524861.1:c.110+1064C>A	XP_011523163.1:n.110+1064C>A