ClinGen Allele Registry
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Canonical Allele Identifier:
CA901420485
Gene: IL12A-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.160001345A>C
GRCh37
chr3:g.159719132A>C
Linked Data - NCBI & NCI
dbSNP:
485497
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.160001345A>C , CM000665.2:g.160001345A>C
GRCh38
NC_000003.11:g.159719132A>C , CM000665.1:g.159719132A>C
GRCh37
NC_000003.10:g.161201826A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_108088.1:n.823-3240T>G
Search 100 bp 5'
Search 100 bp 3'