Canonical Allele Identifier: CA2254022708
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801676_27801677delinsGA , CM000679.2:g.27801676_27801677delinsGA GRCh38
NC_000017.10:g.26128702_26128703delinsGA , CM000679.1:g.26128702_26128703delinsGA GRCh37
NC_000017.9:g.23152829_23152830delinsGA NCBI36
NG_011470.1:g.3853_3854delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2446_438+2447delinsTC ENSP00000462879.1:n.438+2446_438+2447delinsTC
XM_011524859.1:c.-74+2446_-74+2447delinsTC XP_011523161.1:n.-74+2446_-74+2447delinsTC