Canonical Allele Identifier: CA2066046337
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1174932812

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439706C>A , CM000674.2:g.117439706C>A GRCh38
NC_000012.11:g.117877511C>A , CM000674.1:g.117877511C>A GRCh37
NC_000012.10:g.116361894C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11995G>T