Canonical Allele Identifier: CA398317343
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.256G>C ENSP00000462879.1:p.Glu86Gln
XM_011524859.1:c.-256G>C XP_011523161.1:n.-256G>C