Canonical Allele Identifier: CA2733432657
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs2142537078

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801579C>T , CM000679.2:g.27801579C>T GRCh38
NC_000017.10:g.26128605C>T , CM000679.1:g.26128605C>T GRCh37
NC_000017.9:g.23152732C>T NCBI36
NG_011470.1:g.3951G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2544G>A ENSP00000462879.1:n.438+2544G>A
XM_011524859.1:c.-74+2544G>A XP_011523161.1:n.-74+2544G>A