Canonical Allele Identifier: CA2066046396
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1592882389

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439739A>C , CM000674.2:g.117439739A>C GRCh38
NC_000012.11:g.117877544A>C , CM000674.1:g.117877544A>C GRCh37
NC_000012.10:g.116361927A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+11962T>G