Canonical Allele Identifier: CA2066046387
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439731A= , CM000674.2:g.117439731A= GRCh38
NC_000012.11:g.117877536A= , CM000674.1:g.117877536A= GRCh37
NC_000012.10:g.116361919A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+11970T=