ClinGen Allele Registry
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Canonical Allele Identifier:
CA87033642
Gene: IL12A-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.160079403A>T
GRCh37
chr3:g.159797190A>T
Linked Data - Sequence & Population
gnomAD v2:
3:159797190 A / T
gnomAD v3:
3:160079403 A / T
gnomAD v4:
chr3-160079403-A-T
Joint Max Group AF
0.72511025 (AMR)
Genomes Max Group AF
0.72511025 (AMR)
Linked Data - NCBI & NCI
dbSNP:
9847915
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.160079403A>T , CM000665.2:g.160079403A>T
GRCh38
NC_000003.11:g.159797190A>T , CM000665.1:g.159797190A>T
GRCh37
NC_000003.10:g.161279884A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_108088.1:n.518-53869T>A
Search 100 bp 5'
Search 100 bp 3'