Canonical Allele Identifier: CA289077450
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs894432750

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801398G>C , CM000679.2:g.27801398G>C GRCh38
NC_000017.10:g.26128424G>C , CM000679.1:g.26128424G>C GRCh37
NC_000017.9:g.23152551G>C NCBI36
NG_011470.1:g.4132C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.439-2516C>G ENSP00000462879.1:n.439-2516C>G
XM_011524859.1:c.-73-2516C>G XP_011523161.1:n.-73-2516C>G