Canonical Allele Identifier: CA727661056
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1437005465

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801474C>A , CM000679.2:g.27801474C>A GRCh38
NC_000017.10:g.26128500C>A , CM000679.1:g.26128500C>A GRCh37
NC_000017.9:g.23152627C>A NCBI36
NG_011470.1:g.4056G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2592G>T ENSP00000462879.1:n.439-2592G>T
XM_011524859.1:c.-73-2592G>T XP_011523161.1:n.-73-2592G>T