Canonical Allele Identifier: CA398317023
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131243C>T (hg19) chr17:g.27804217C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804217C>T , CM000679.2:g.27804217C>T GRCh38
NC_000017.10:g.26131243C>T , CM000679.1:g.26131243C>T GRCh37
NC_000017.9:g.23155370C>T NCBI36
NG_011470.1:g.1313G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.344G>A ENSP00000462879.1:p.Gly115Glu
XM_011524859.1:c.-168G>A XP_011523161.1:n.-168G>A
Search 100 bp 5'
Search 100 bp 3'