Canonical Allele Identifier: CA14375587
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs2779249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801555C>A , CM000679.2:g.27801555C>A GRCh38
NC_000017.10:g.26128581C>A , CM000679.1:g.26128581C>A GRCh37
NC_000017.9:g.23152708C>A NCBI36
NG_011470.1:g.3975G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2568G>T ENSP00000462879.1:n.438+2568G>T
XM_011524859.1:c.-74+2568G>T XP_011523161.1:n.-74+2568G>T