Canonical Allele Identifier: CA684138796
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1236538922

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439714del , CM000674.2:g.117439714del GRCh38
NC_000012.11:g.117877519del , CM000674.1:g.117877519del GRCh37
NC_000012.10:g.116361902del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11987del