Canonical Allele Identifier: CA398317318
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804300G>C , CM000679.2:g.27804300G>C GRCh38
NC_000017.10:g.26131326G>C , CM000679.1:g.26131326G>C GRCh37
NC_000017.9:g.23155453G>C NCBI36
NG_011470.1:g.1230C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.261C>G ENSP00000462879.1:p.Cys87Trp
XM_011524859.1:c.-251C>G XP_011523161.1:n.-251C>G