Canonical Allele Identifier: CA398317026
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804218C>G , CM000679.2:g.27804218C>G GRCh38
NC_000017.10:g.26131244C>G , CM000679.1:g.26131244C>G GRCh37
NC_000017.9:g.23155371C>G NCBI36
NG_011470.1:g.1312G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.343G>C ENSP00000462879.1:p.Gly115Arg
XM_011524859.1:c.-169G>C XP_011523161.1:n.-169G>C