Canonical Allele Identifier: CA2809098602
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801669G>A , CM000679.2:g.27801669G>A GRCh38
NC_000017.10:g.26128695G>A , CM000679.1:g.26128695G>A GRCh37
NC_000017.9:g.23152822G>A NCBI36
NG_011470.1:g.3861C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2454C>T ENSP00000462879.1:n.438+2454C>T
XM_011524859.1:c.-74+2454C>T XP_011523161.1:n.-74+2454C>T