Canonical Allele Identifier: CA398317427
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131352A>C (hg19) chr17:g.27804326A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804326A>C , CM000679.2:g.27804326A>C GRCh38
NC_000017.10:g.26131352A>C , CM000679.1:g.26131352A>C GRCh37
NC_000017.9:g.23155479A>C NCBI36
NG_011470.1:g.1204T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.235T>G ENSP00000462879.1:p.Ser79Ala
XM_011524859.1:c.-277T>G XP_011523161.1:n.-277T>G
Search 100 bp 5'
Search 100 bp 3'