Canonical Allele Identifier: CA2254022650
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801531G= , CM000679.2:g.27801531G= GRCh38
NC_000017.10:g.26128557G= , CM000679.1:g.26128557G= GRCh37
NC_000017.9:g.23152684G= NCBI36
NG_011470.1:g.3999C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2592C= ENSP00000462879.1:n.438+2592C=
XM_011524859.1:c.-74+2592C= XP_011523161.1:n.-74+2592C=