Canonical Allele Identifier: CA982708871
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909547619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801433T>C , CM000679.2:g.27801433T>C GRCh38
NC_000017.10:g.26128459T>C , CM000679.1:g.26128459T>C GRCh37
NC_000017.9:g.23152586T>C NCBI36
NG_011470.1:g.4097A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.439-2551A>G ENSP00000462879.1:n.439-2551A>G
XM_011524859.1:c.-73-2551A>G XP_011523161.1:n.-73-2551A>G