Canonical Allele Identifier: CA289077587
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs570471922

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801683dup , CM000679.2:g.27801683dup GRCh38
NC_000017.10:g.26128709dup , CM000679.1:g.26128709dup GRCh37
NC_000017.9:g.23152836dup NCBI36
NG_011470.1:g.3853dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2446dup ENSP00000462879.1:n.438+2446dup
XM_011524859.1:c.-74+2446dup XP_011523161.1:n.-74+2446dup