Canonical Allele Identifier: CA2066046366
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1592882386

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439721T>G , CM000674.2:g.117439721T>G GRCh38
NC_000012.11:g.117877526T>G , CM000674.1:g.117877526T>G GRCh37
NC_000012.10:g.116361909T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11980A>C