Canonical Allele Identifier: CA2066046392
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439732C= , CM000674.2:g.117439732C= GRCh38
NC_000012.11:g.117877537C= , CM000674.1:g.117877537C= GRCh37
NC_000012.10:g.116361920C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11969G=