Canonical Allele Identifier: CA2066046348
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439713_117439714delinsCA , CM000674.2:g.117439713_117439714delinsCA GRCh38
NC_000012.11:g.117877518_117877519delinsCA , CM000674.1:g.117877518_117877519delinsCA GRCh37
NC_000012.10:g.116361901_116361902delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11987_470+11988delinsTG