Canonical Allele Identifier: CA398317057
Gene: NOS2 HGNC NCBI

Linked Data

gnomAD v4: 17-27804226-A-G
MyVariant Identifiers: chr17:g.26131252A>G (hg19) chr17:g.27804226A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804226A>G , CM000679.2:g.27804226A>G GRCh38
NC_000017.10:g.26131252A>G , CM000679.1:g.26131252A>G GRCh37
NC_000017.9:g.23155379A>G NCBI36
NG_011470.1:g.1304T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.335T>C ENSP00000462879.1:p.Leu112Pro
XM_011524859.1:c.-177T>C XP_011523161.1:n.-177T>C
Search 100 bp 5'
Search 100 bp 3'