Canonical Allele Identifier: CA398317228
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131302T>A (hg19) chr17:g.27804276T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804276T>A , CM000679.2:g.27804276T>A GRCh38
NC_000017.10:g.26131302T>A , CM000679.1:g.26131302T>A GRCh37
NC_000017.9:g.23155429T>A NCBI36
NG_011470.1:g.1254A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.285A>T ENSP00000462879.1:p.Gln95His
XM_011524859.1:c.-227A>T XP_011523161.1:n.-227A>T
Search 100 bp 5'
Search 100 bp 3'