Canonical Allele Identifier: CA727661061
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1333409249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801479T>G , CM000679.2:g.27801479T>G GRCh38
NC_000017.10:g.26128505T>G , CM000679.1:g.26128505T>G GRCh37
NC_000017.9:g.23152632T>G NCBI36
NG_011470.1:g.4051A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2597A>C ENSP00000462879.1:n.439-2597A>C
XM_011524859.1:c.-73-2597A>C XP_011523161.1:n.-73-2597A>C