Canonical Allele Identifier: CA2254023858
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804244C= , CM000679.2:g.27804244C= GRCh38
NC_000017.10:g.26131270C= , CM000679.1:g.26131270C= GRCh37
NC_000017.9:g.23155397C= NCBI36
NG_011470.1:g.1286G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.317G= ENSP00000462879.1:p.Arg106=
XM_011524859.1:c.-195G= XP_011523161.1:n.-195G=