Canonical Allele Identifier: CA398316634
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804127G>T , CM000679.2:g.27804127G>T GRCh38
NC_000017.10:g.26131153G>T , CM000679.1:g.26131153G>T GRCh37
NC_000017.9:g.23155280G>T NCBI36
NG_011470.1:g.1403C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.434C>A ENSP00000462879.1:p.Thr145Asn
XM_011524859.1:c.-78C>A XP_011523161.1:n.-78C>A