Canonical Allele Identifier: CA2254022622
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801479T= , CM000679.2:g.27801479T= GRCh38
NC_000017.10:g.26128505T= , CM000679.1:g.26128505T= GRCh37
NC_000017.9:g.23152632T= NCBI36
NG_011470.1:g.4051A=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2597A= ENSP00000462879.1:n.439-2597A=
XM_011524859.1:c.-73-2597A= XP_011523161.1:n.-73-2597A=