Canonical Allele Identifier: CA2254023823
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804116G= , CM000679.2:g.27804116G= GRCh38
NC_000017.10:g.26131142G= , CM000679.1:g.26131142G= GRCh37
NC_000017.9:g.23155269G= NCBI36
NG_011470.1:g.1414C=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+7C= ENSP00000462879.1:n.438+7C=
XM_011524859.1:c.-74+7C= XP_011523161.1:n.-74+7C=