Canonical Allele Identifier: CA2809098596
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801579C>A , CM000679.2:g.27801579C>A GRCh38
NC_000017.10:g.26128605C>A , CM000679.1:g.26128605C>A GRCh37
NC_000017.9:g.23152732C>A NCBI36
NG_011470.1:g.3951G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2544G>T ENSP00000462879.1:n.438+2544G>T
XM_011524859.1:c.-74+2544G>T XP_011523161.1:n.-74+2544G>T