ClinGen Allele Registry
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Canonical Allele Identifier:
CA87002477
Gene: IL12A-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.159947262A>G
GRCh37
chr3:g.159665050A>G
Linked Data - Sequence & Population
gnomAD v2:
3:159665050 A / G
gnomAD v3:
3:159947262 A / G
gnomAD v4:
chr3-159947262-A-G
Joint Max Group AF
0.11948428 (NFE)
Genomes Max Group AF
0.11948428 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17810546
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.159947262A>G , CM000665.2:g.159947262A>G
GRCh38
NC_000003.11:g.159665050A>G , CM000665.1:g.159665050A>G
GRCh37
NC_000003.10:g.161147744A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_108088.1:n.1351-32788T>C
Search 100 bp 5'
Search 100 bp 3'