Canonical Allele Identifier: CA398317395
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131345A>C (hg19) chr17:g.27804319A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804319A>C , CM000679.2:g.27804319A>C GRCh38
NC_000017.10:g.26131345A>C , CM000679.1:g.26131345A>C GRCh37
NC_000017.9:g.23155472A>C NCBI36
NG_011470.1:g.1211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.242T>G ENSP00000462879.1:p.Ile81Ser
XM_011524859.1:c.-270T>G XP_011523161.1:n.-270T>G
Search 100 bp 5'
Search 100 bp 3'