Canonical Allele Identifier: CA2066046306
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1870090631

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439692G>A , CM000674.2:g.117439692G>A GRCh38
NC_000012.11:g.117877497G>A , CM000674.1:g.117877497G>A GRCh37
NC_000012.10:g.116361880G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12009C>T