Canonical Allele Identifier: CA289078707
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1004244229
gnomAD v3: 17-27804320-T-C
gnomAD v4: 17-27804320-T-C
MyVariant Identifiers: chr17:g.26131346T>C (hg19) chr17:g.27804320T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804320T>C , CM000679.2:g.27804320T>C GRCh38
NC_000017.10:g.26131346T>C , CM000679.1:g.26131346T>C GRCh37
NC_000017.9:g.23155473T>C NCBI36
NG_011470.1:g.1210A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.241A>G ENSP00000462879.1:p.Ile81Val
XM_011524859.1:c.-271A>G XP_011523161.1:n.-271A>G
Search 100 bp 5'
Search 100 bp 3'