Canonical Allele Identifier: CA2254020819

Gene: NOS2

Linked Data

• dbSNP Id: rs1909389278
• gnomAD v3: 17-27797541-T-G
• gnomAD v4: 17-27797541-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27797541T>G , CM000679.2:g.27797541T>G	GRCh38
NC_000017.10:g.26124567T>G , CM000679.1:g.26124567T>G	GRCh37
NC_000017.9:g.23148694T>G	NCBI36
NG_011470.1:g.7989A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.110+1159A>C	ENSP00000513259.1:n.110+1159A>C
ENST00000313735.11:c.110+1159A>C MANE Select	ENSP00000327251.6:n.110+1159A>C
ENST00000313735.10:c.110+1159A>C	ENSP00000327251.6:n.110+1159A>C
ENST00000621962.1:c.110+1159A>C	ENSP00000482291.1:n.110+1159A>C
NM_000625.4:c.110+1159A>C MANE Select	NP_000616.3:n.110+1159A>C
XM_011524859.1:c.110+1159A>C	XP_011523161.1:n.110+1159A>C
XM_011524861.1:c.110+1159A>C	XP_011523163.1:n.110+1159A>C