Canonical Allele Identifier: CA727661085
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1440777257

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801524dup , CM000679.2:g.27801524dup GRCh38
NC_000017.10:g.26128550dup , CM000679.1:g.26128550dup GRCh37
NC_000017.9:g.23152677dup NCBI36
NG_011470.1:g.4006dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2599dup ENSP00000462879.1:n.438+2599dup
XM_011524859.1:c.-74+2599dup XP_011523161.1:n.-74+2599dup