Canonical Allele Identifier: CA2254022654
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801544G= , CM000679.2:g.27801544G= GRCh38
NC_000017.10:g.26128570G= , CM000679.1:g.26128570G= GRCh37
NC_000017.9:g.23152697G= NCBI36
NG_011470.1:g.3986C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2579C= ENSP00000462879.1:n.438+2579C=
XM_011524859.1:c.-74+2579C= XP_011523161.1:n.-74+2579C=