Canonical Allele Identifier: CA2809098603
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801670C>A , CM000679.2:g.27801670C>A GRCh38
NC_000017.10:g.26128696C>A , CM000679.1:g.26128696C>A GRCh37
NC_000017.9:g.23152823C>A NCBI36
NG_011470.1:g.3860G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2453G>T ENSP00000462879.1:n.438+2453G>T
XM_011524859.1:c.-74+2453G>T XP_011523161.1:n.-74+2453G>T