Canonical Allele Identifier: CA245041522

Gene: NOS1

Linked Data

• dbSNP Id: rs983042416
• MyVariant Identifiers: chr12:g.117877414G>T (hg19) ; chr12:g.117439609G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117439609G>T , CM000674.2:g.117439609G>T	GRCh38
NC_000012.11:g.117877414G>T , CM000674.1:g.117877414G>T	GRCh37
NC_000012.10:g.116361797G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549189.1:n.470+12092C>A