Canonical Allele Identifier: CA2254023853
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804225G= , CM000679.2:g.27804225G= GRCh38
NC_000017.10:g.26131251G= , CM000679.1:g.26131251G= GRCh37
NC_000017.9:g.23155378G= NCBI36
NG_011470.1:g.1305C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.336C= ENSP00000462879.1:p.Leu112=
XM_011524859.1:c.-176C= XP_011523161.1:n.-176C=