Canonical Allele Identifier: CA2733288651
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909555702

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801568T>C , CM000679.2:g.27801568T>C GRCh38
NC_000017.10:g.26128594T>C , CM000679.1:g.26128594T>C GRCh37
NC_000017.9:g.23152721T>C NCBI36
NG_011470.1:g.3962A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2555A>G ENSP00000462879.1:n.438+2555A>G
XM_011524859.1:c.-74+2555A>G XP_011523161.1:n.-74+2555A>G