Canonical Allele Identifier: CA398317369
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804312T>A , CM000679.2:g.27804312T>A GRCh38
NC_000017.10:g.26131338T>A , CM000679.1:g.26131338T>A GRCh37
NC_000017.9:g.23155465T>A NCBI36
NG_011470.1:g.1218A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.249A>T ENSP00000462879.1:p.Arg83Ser
XM_011524859.1:c.-263A>T XP_011523161.1:n.-263A>T