Canonical Allele Identifier: CA398317340
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909651495

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.256G>T ENSP00000462879.1:p.Glu86Ter
XM_011524859.1:c.-256G>T XP_011523161.1:n.-256G>T