Canonical Allele Identifier: CA982708859
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909543564
gnomAD v3: 17-27801366-C-T
gnomAD v4: 17-27801366-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801366C>T , CM000679.2:g.27801366C>T GRCh38
NC_000017.10:g.26128392C>T , CM000679.1:g.26128392C>T GRCh37
NC_000017.9:g.23152519C>T NCBI36
NG_011470.1:g.4164G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2484G>A ENSP00000462879.1:n.439-2484G>A
XM_011524859.1:c.-73-2484G>A XP_011523161.1:n.-73-2484G>A
Search 100 bp 5'
Search 100 bp 3'