Canonical Allele Identifier: CA727661030
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1455003347

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801404C>T , CM000679.2:g.27801404C>T GRCh38
NC_000017.10:g.26128430C>T , CM000679.1:g.26128430C>T GRCh37
NC_000017.9:g.23152557C>T NCBI36
NG_011470.1:g.4126G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.439-2522G>A ENSP00000462879.1:n.439-2522G>A
XM_011524859.1:c.-73-2522G>A XP_011523161.1:n.-73-2522G>A