Allele Registry

Canonical Allele Identifier: CA11560344

Gene: IL12A-AS1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.159981157T>C

GRCh37 chr3:g.159698945T>C

Linked Data - Sequence & Population

gnomAD v2:

3:159698945 T / C

gnomAD v3:

3:159981157 T / C

gnomAD v4:

chr3-159981157-T-C

Joint Max Group AF 0.44130146 (AFR)

Genomes Max Group AF 0.44130146 (AFR)

Linked Data - NCBI & NCI

dbSNP:

4680534

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.159981157T>C , CM000665.2:g.159981157T>C	GRCh38
NC_000003.11:g.159698945T>C , CM000665.1:g.159698945T>C	GRCh37
NC_000003.10:g.161181639T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_108088.1:n.1350+7940A>G

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