Canonical Allele Identifier: CA2254023819
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804110T= , CM000679.2:g.27804110T= GRCh38
NC_000017.10:g.26131136T= , CM000679.1:g.26131136T= GRCh37
NC_000017.9:g.23155263T= NCBI36
NG_011470.1:g.1420A=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+13A= ENSP00000462879.1:n.438+13A=
XM_011524859.1:c.-74+13A= XP_011523161.1:n.-74+13A=