Canonical Allele Identifier: CA498791668
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909651681
MyVariant Identifiers: chr17:g.26131335G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804309G>A , CM000679.2:g.27804309G>A GRCh38
NC_000017.10:g.26131335G>A , CM000679.1:g.26131335G>A GRCh37
NC_000017.9:g.23155462G>A NCBI36
NG_011470.1:g.1221C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.252C>T ENSP00000462879.1:p.Gly84=
XM_011524859.1:c.-260C>T XP_011523161.1:n.-260C>T