Canonical Allele Identifier: CA2254022670
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909555702

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801568T>A , CM000679.2:g.27801568T>A GRCh38
NC_000017.10:g.26128594T>A , CM000679.1:g.26128594T>A GRCh37
NC_000017.9:g.23152721T>A NCBI36
NG_011470.1:g.3962A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2555A>T ENSP00000462879.1:n.438+2555A>T
XM_011524859.1:c.-74+2555A>T XP_011523161.1:n.-74+2555A>T