Canonical Allele Identifier: CA398317059
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804226A>T , CM000679.2:g.27804226A>T GRCh38
NC_000017.10:g.26131252A>T , CM000679.1:g.26131252A>T GRCh37
NC_000017.9:g.23155379A>T NCBI36
NG_011470.1:g.1304T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.335T>A ENSP00000462879.1:p.Leu112His
XM_011524859.1:c.-177T>A XP_011523161.1:n.-177T>A