Canonical Allele Identifier: CA289077562
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs559659979

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801584A>G , CM000679.2:g.27801584A>G GRCh38
NC_000017.10:g.26128610A>G , CM000679.1:g.26128610A>G GRCh37
NC_000017.9:g.23152737A>G NCBI36
NG_011470.1:g.3946T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2539T>C ENSP00000462879.1:n.438+2539T>C
XM_011524859.1:c.-74+2539T>C XP_011523161.1:n.-74+2539T>C