Canonical Allele Identifier: CA498790004
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131155C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804129C>T , CM000679.2:g.27804129C>T GRCh38
NC_000017.10:g.26131155C>T , CM000679.1:g.26131155C>T GRCh37
NC_000017.9:g.23155282C>T NCBI36
NG_011470.1:g.1401G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.432G>A ENSP00000462879.1:p.Val144=
XM_011524859.1:c.-80G>A XP_011523161.1:n.-80G>A
Search 100 bp 5'
Search 100 bp 3'