Canonical Allele Identifier: CA2066046051
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439559C= , CM000674.2:g.117439559C= GRCh38
NC_000012.11:g.117877364C= , CM000674.1:g.117877364C= GRCh37
NC_000012.10:g.116361747C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+12142G=