Canonical Allele Identifier: CA2254022704
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801656G= , CM000679.2:g.27801656G= GRCh38
NC_000017.10:g.26128682G= , CM000679.1:g.26128682G= GRCh37
NC_000017.9:g.23152809G= NCBI36
NG_011470.1:g.3874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2467C= ENSP00000462879.1:n.438+2467C=
XM_011524859.1:c.-74+2467C= XP_011523161.1:n.-74+2467C=