Canonical Allele Identifier: CA398317370
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804312T>G , CM000679.2:g.27804312T>G GRCh38
NC_000017.10:g.26131338T>G , CM000679.1:g.26131338T>G GRCh37
NC_000017.9:g.23155465T>G NCBI36
NG_011470.1:g.1218A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.249A>C ENSP00000462879.1:p.Arg83Ser
XM_011524859.1:c.-263A>C XP_011523161.1:n.-263A>C