Canonical Allele Identifier: CA2066046330
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439705_117439706delinsGC , CM000674.2:g.117439705_117439706delinsGC GRCh38
NC_000012.11:g.117877510_117877511delinsGC , CM000674.1:g.117877510_117877511delinsGC GRCh37
NC_000012.10:g.116361893_116361894delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11995_470+11996delinsGC