Canonical Allele Identifier: CA8455218
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2779251

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804300G>A , CM000679.2:g.27804300G>A GRCh38
NC_000017.10:g.26131326G>A , CM000679.1:g.26131326G>A GRCh37
NC_000017.9:g.23155453G>A NCBI36
NG_011470.1:g.1230C>T

Transcript Alleles

HGVS Amino-acid change
XM_011524859.1:c.-251C>T XP_011523161.1:p.=
ENST00000582441.1:c.261C>T ENSP00000462879.1:p.Cys87=