Canonical Allele Identifier: CA498789948
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131152G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804126G>A , CM000679.2:g.27804126G>A GRCh38
NC_000017.10:g.26131152G>A , CM000679.1:g.26131152G>A GRCh37
NC_000017.9:g.23155279G>A NCBI36
NG_011470.1:g.1404C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.435C>T ENSP00000462879.1:p.Thr145=
XM_011524859.1:c.-77C>T XP_011523161.1:n.-77C>T