Canonical Allele Identifier: CA289077841
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27802186G>A , CM000679.2:g.27802186G>A GRCh38
NC_000017.10:g.26129212G>A , CM000679.1:g.26129212G>A GRCh37
NC_000017.9:g.23153339G>A NCBI36
NG_011470.1:g.3344C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+1937C>T ENSP00000462879.1:n.438+1937C>T
XM_011524859.1:c.-74+1937C>T XP_011523161.1:n.-74+1937C>T