Canonical Allele Identifier: CA2066046370
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1592882387

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439724C>A , CM000674.2:g.117439724C>A GRCh38
NC_000012.11:g.117877529C>A , CM000674.1:g.117877529C>A GRCh37
NC_000012.10:g.116361912C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+11977G>T