Canonical Allele Identifier: CA289077517
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1017541736

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801485C>T , CM000679.2:g.27801485C>T GRCh38
NC_000017.10:g.26128511C>T , CM000679.1:g.26128511C>T GRCh37
NC_000017.9:g.23152638C>T NCBI36
NG_011470.1:g.4045G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2603G>A ENSP00000462879.1:n.439-2603G>A
XM_011524859.1:c.-73-2603G>A XP_011523161.1:n.-73-2603G>A