Canonical Allele Identifier: CA289077575
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs533546624

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801608T>C , CM000679.2:g.27801608T>C GRCh38
NC_000017.10:g.26128634T>C , CM000679.1:g.26128634T>C GRCh37
NC_000017.9:g.23152761T>C NCBI36
NG_011470.1:g.3922A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+2515A>G ENSP00000462879.1:n.438+2515A>G
XM_011524859.1:c.-74+2515A>G XP_011523161.1:n.-74+2515A>G