Canonical Allele Identifier: CA498789911
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131149C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804123C>T , CM000679.2:g.27804123C>T GRCh38
NC_000017.10:g.26131149C>T , CM000679.1:g.26131149C>T GRCh37
NC_000017.9:g.23155276C>T NCBI36
NG_011470.1:g.1407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438G>A ENSP00000462879.1:p.Leu146=
XM_011524859.1:c.-74G>A XP_011523161.1:n.-74G>A
Search 100 bp 5'
Search 100 bp 3'