Canonical Allele Identifier: CA398316988
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804208G>T , CM000679.2:g.27804208G>T GRCh38
NC_000017.10:g.26131234G>T , CM000679.1:g.26131234G>T GRCh37
NC_000017.9:g.23155361G>T NCBI36
NG_011470.1:g.1322C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.353C>A ENSP00000462879.1:p.Pro118His
XM_011524859.1:c.-159C>A XP_011523161.1:n.-159C>A