Canonical Allele Identifier: CA2254022634
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909551853

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801497C>A , CM000679.2:g.27801497C>A GRCh38
NC_000017.10:g.26128523C>A , CM000679.1:g.26128523C>A GRCh37
NC_000017.9:g.23152650C>A NCBI36
NG_011470.1:g.4033G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2615G>T ENSP00000462879.1:n.439-2615G>T
XM_011524859.1:c.-73-2615G>T XP_011523161.1:n.-73-2615G>T