Canonical Allele Identifier: CA2254022696
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801613A= , CM000679.2:g.27801613A= GRCh38
NC_000017.10:g.26128639A= , CM000679.1:g.26128639A= GRCh37
NC_000017.9:g.23152766A= NCBI36
NG_011470.1:g.3917T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2510T= ENSP00000462879.1:n.438+2510T=
XM_011524859.1:c.-74+2510T= XP_011523161.1:n.-74+2510T=