ClinGen Allele Registry
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Canonical Allele Identifier:
CA607800317
Gene: NOS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1309552584
gnomAD v2:
12-117877408-C-T
gnomAD v3:
12-117439603-C-T
gnomAD v4:
12-117439603-C-T
MyVariant Identifiers:
chr12:g.117877408C>T (hg19)
chr12:g.117439603C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.117439603C>T , CM000674.2:g.117439603C>T
GRCh38
NC_000012.11:g.117877408C>T , CM000674.1:g.117877408C>T
GRCh37
NC_000012.10:g.116361791C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000549189.1:n.470+12098G>A
Search 100 bp 5'
Search 100 bp 3'