Canonical Allele Identifier: CA2254022621
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801478C= , CM000679.2:g.27801478C= GRCh38
NC_000017.10:g.26128504C= , CM000679.1:g.26128504C= GRCh37
NC_000017.9:g.23152631C= NCBI36
NG_011470.1:g.4052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2596G= ENSP00000462879.1:n.439-2596G=
XM_011524859.1:c.-73-2596G= XP_011523161.1:n.-73-2596G=