Canonical Allele Identifier: CA245041550
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs977055605
MyVariant Identifiers: chr12:g.117877551G>C (hg19) chr12:g.117439746G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439746G>C , CM000674.2:g.117439746G>C GRCh38
NC_000012.11:g.117877551G>C , CM000674.1:g.117877551G>C GRCh37
NC_000012.10:g.116361934G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+11955C>G
Search 100 bp 5'
Search 100 bp 3'