Canonical Allele Identifier: CA2254023885
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804320T= , CM000679.2:g.27804320T= GRCh38
NC_000017.10:g.26131346T= , CM000679.1:g.26131346T= GRCh37
NC_000017.9:g.23155473T= NCBI36
NG_011470.1:g.1210A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.241A= ENSP00000462879.1:p.Ile81=
XM_011524859.1:c.-271A= XP_011523161.1:n.-271A=