Canonical Allele Identifier: CA727658961

Gene: NOS2

Linked Data

• dbSNP Id: rs1289869572
• gnomAD v3: 17-27797614-A-G
• gnomAD v4: 17-27797614-A-G
• MyVariant Identifiers: chr17:g.26124640A>G (hg19) ; chr17:g.27797614A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27797614A>G , CM000679.2:g.27797614A>G	GRCh38
NC_000017.10:g.26124640A>G , CM000679.1:g.26124640A>G	GRCh37
NC_000017.9:g.23148767A>G	NCBI36
NG_011470.1:g.7916T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.110+1086T>C	ENSP00000513259.1:n.110+1086T>C
ENST00000313735.11:c.110+1086T>C MANE Select	ENSP00000327251.6:n.110+1086T>C
ENST00000313735.10:c.110+1086T>C	ENSP00000327251.6:n.110+1086T>C
ENST00000621962.1:c.110+1086T>C	ENSP00000482291.1:n.110+1086T>C
NM_000625.4:c.110+1086T>C MANE Select	NP_000616.3:n.110+1086T>C
XM_011524859.1:c.110+1086T>C	XP_011523161.1:n.110+1086T>C
XM_011524861.1:c.110+1086T>C	XP_011523163.1:n.110+1086T>C