Canonical Allele Identifier: CA398317375
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804313C>A , CM000679.2:g.27804313C>A GRCh38
NC_000017.10:g.26131339C>A , CM000679.1:g.26131339C>A GRCh37
NC_000017.9:g.23155466C>A NCBI36
NG_011470.1:g.1217G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.248G>T ENSP00000462879.1:p.Arg83Ile
XM_011524859.1:c.-264G>T XP_011523161.1:n.-264G>T