Canonical Allele Identifier: CA2254022632
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801496G= , CM000679.2:g.27801496G= GRCh38
NC_000017.10:g.26128522G= , CM000679.1:g.26128522G= GRCh37
NC_000017.9:g.23152649G= NCBI36
NG_011470.1:g.4034C=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2614C= ENSP00000462879.1:n.439-2614C=
XM_011524859.1:c.-73-2614C= XP_011523161.1:n.-73-2614C=