Canonical Allele Identifier: CA607800316
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1270953082

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439599C>G , CM000674.2:g.117439599C>G GRCh38
NC_000012.11:g.117877404C>G , CM000674.1:g.117877404C>G GRCh37
NC_000012.10:g.116361787C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12102G>C