Canonical Allele Identifier: CA398316647
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804130A>C , CM000679.2:g.27804130A>C GRCh38
NC_000017.10:g.26131156A>C , CM000679.1:g.26131156A>C GRCh37
NC_000017.9:g.23155283A>C NCBI36
NG_011470.1:g.1400T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.431T>G ENSP00000462879.1:p.Val144Gly
XM_011524859.1:c.-81T>G XP_011523161.1:n.-81T>G