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Canonical Allele Identifier:
CA11426066
Gene: IL12A-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.160015196T>C
GRCh37
chr3:g.159732983T>C
Linked Data - Sequence & Population
gnomAD v2:
3:159732983 T / C
gnomAD v3:
3:160015196 T / C
gnomAD v4:
chr3-160015196-T-C
Joint Max Group AF
0.46475397 (AFR)
Genomes Max Group AF
0.46475397 (AFR)
Linked Data - NCBI & NCI
dbSNP:
574808
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.160015196T>C , CM000665.2:g.160015196T>C
GRCh38
NC_000003.11:g.159732983T>C , CM000665.1:g.159732983T>C
GRCh37
NC_000003.10:g.161215677T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_108088.1:n.583-5939A>G
Search 100 bp 5'
Search 100 bp 3'