Canonical Allele Identifier: CA245041519
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs570456660

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439586C>T , CM000674.2:g.117439586C>T GRCh38
NC_000012.11:g.117877391C>T , CM000674.1:g.117877391C>T GRCh37
NC_000012.10:g.116361774C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12115G>A