Canonical Allele Identifier: CA2254022603
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801438G= , CM000679.2:g.27801438G= GRCh38
NC_000017.10:g.26128464G= , CM000679.1:g.26128464G= GRCh37
NC_000017.9:g.23152591G= NCBI36
NG_011470.1:g.4092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.439-2556C= ENSP00000462879.1:n.439-2556C=
XM_011524859.1:c.-73-2556C= XP_011523161.1:n.-73-2556C=