Canonical Allele Identifier: CA398317420
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131351G>C (hg19) chr17:g.27804325G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804325G>C , CM000679.2:g.27804325G>C GRCh38
NC_000017.10:g.26131351G>C , CM000679.1:g.26131351G>C GRCh37
NC_000017.9:g.23155478G>C NCBI36
NG_011470.1:g.1205C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.236C>G ENSP00000462879.1:p.Ser79Cys
XM_011524859.1:c.-276C>G XP_011523161.1:n.-276C>G
Search 100 bp 5'
Search 100 bp 3'