Canonical Allele Identifier: CA289077563
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs915575196

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801597C>T , CM000679.2:g.27801597C>T GRCh38
NC_000017.10:g.26128623C>T , CM000679.1:g.26128623C>T GRCh37
NC_000017.9:g.23152750C>T NCBI36
NG_011470.1:g.3933G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2526G>A ENSP00000462879.1:n.438+2526G>A
XM_011524859.1:c.-74+2526G>A XP_011523161.1:n.-74+2526G>A