Canonical Allele Identifier: CA398317352
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804307T>C , CM000679.2:g.27804307T>C GRCh38
NC_000017.10:g.26131333T>C , CM000679.1:g.26131333T>C GRCh37
NC_000017.9:g.23155460T>C NCBI36
NG_011470.1:g.1223A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.254A>G ENSP00000462879.1:p.Gln85Arg
XM_011524859.1:c.-258A>G XP_011523161.1:n.-258A>G