Canonical Allele Identifier: CA2254022671
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801572T= , CM000679.2:g.27801572T= GRCh38
NC_000017.10:g.26128598T= , CM000679.1:g.26128598T= GRCh37
NC_000017.9:g.23152725T= NCBI36
NG_011470.1:g.3958A=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2551A= ENSP00000462879.1:n.438+2551A=
XM_011524859.1:c.-74+2551A= XP_011523161.1:n.-74+2551A=