Canonical Allele Identifier: CA398317331
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804303T>A , CM000679.2:g.27804303T>A GRCh38
NC_000017.10:g.26131329T>A , CM000679.1:g.26131329T>A GRCh37
NC_000017.9:g.23155456T>A NCBI36
NG_011470.1:g.1227A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.258A>T ENSP00000462879.1:p.Glu86Asp
XM_011524859.1:c.-254A>T XP_011523161.1:n.-254A>T