Canonical Allele Identifier: CA398317367
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804311C>G , CM000679.2:g.27804311C>G GRCh38
NC_000017.10:g.26131337C>G , CM000679.1:g.26131337C>G GRCh37
NC_000017.9:g.23155464C>G NCBI36
NG_011470.1:g.1219G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.250G>C ENSP00000462879.1:p.Gly84Arg
XM_011524859.1:c.-262G>C XP_011523161.1:n.-262G>C