Canonical Allele Identifier: CA727661159
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs570471922

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801683del , CM000679.2:g.27801683del GRCh38
NC_000017.10:g.26128709del , CM000679.1:g.26128709del GRCh37
NC_000017.9:g.23152836del NCBI36
NG_011470.1:g.3853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2446del ENSP00000462879.1:n.438+2446del
XM_011524859.1:c.-74+2446del XP_011523161.1:n.-74+2446del