Canonical Allele Identifier: CA2254022686
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801602T= , CM000679.2:g.27801602T= GRCh38
NC_000017.10:g.26128628T= , CM000679.1:g.26128628T= GRCh37
NC_000017.9:g.23152755T= NCBI36
NG_011470.1:g.3928A=

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2521A= ENSP00000462879.1:n.438+2521A=
XM_011524859.1:c.-74+2521A= XP_011523161.1:n.-74+2521A=