Canonical Allele Identifier: CA2066046371
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1592882387

Genomic Alleles

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

Transcript Alleles

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