Canonical Allele Identifier: CA2254023880
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804308G= , CM000679.2:g.27804308G= GRCh38
NC_000017.10:g.26131334G= , CM000679.1:g.26131334G= GRCh37
NC_000017.9:g.23155461G= NCBI36
NG_011470.1:g.1222C=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.253C= ENSP00000462879.1:p.Gln85=
XM_011524859.1:c.-259C= XP_011523161.1:n.-259C=