Canonical Allele Identifier: CA727661143

Gene: NOS2

Linked Data

• dbSNP Id: rs1361948508
• gnomAD v3: 17-27801613-A-G
• gnomAD v4: 17-27801613-A-G
• MyVariant Identifiers: chr17:g.26128639A>G (hg19) ; chr17:g.27801613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27801613A>G , CM000679.2:g.27801613A>G	GRCh38
NC_000017.10:g.26128639A>G , CM000679.1:g.26128639A>G	GRCh37
NC_000017.9:g.23152766A>G	NCBI36
NG_011470.1:g.3917T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000582441.1:c.438+2510T>C	ENSP00000462879.1:n.438+2510T>C
XM_011524859.1:c.-74+2510T>C	XP_011523161.1:n.-74+2510T>C