Canonical Allele Identifier: CA398317425
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804326A>T , CM000679.2:g.27804326A>T GRCh38
NC_000017.10:g.26131352A>T , CM000679.1:g.26131352A>T GRCh37
NC_000017.9:g.23155479A>T NCBI36
NG_011470.1:g.1204T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.235T>A ENSP00000462879.1:p.Ser79Thr
XM_011524859.1:c.-277T>A XP_011523161.1:n.-277T>A