Canonical Allele Identifier: CA2254023878
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804305C= , CM000679.2:g.27804305C= GRCh38
NC_000017.10:g.26131331C= , CM000679.1:g.26131331C= GRCh37
NC_000017.9:g.23155458C= NCBI36
NG_011470.1:g.1225G=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.256G= ENSP00000462879.1:p.Glu86=
XM_011524859.1:c.-256G= XP_011523161.1:n.-256G=