ClinGen Allele Registry
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Canonical Allele Identifier:
CA11816770
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.141807619G>C
GRCh37
chr4:g.142728772G>C
Linked Data - Sequence & Population
gnomAD v2:
4:142728772 G / C
gnomAD v3:
4:141807619 G / C
gnomAD v4:
chr4-141807619-G-C
Joint Max Group AF
0.48258469 (EAS)
Genomes Max Group AF
0.48258469 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17015014
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.141807619G>C , CM000666.2:g.141807619G>C
GRCh38
NC_000004.11:g.142728772G>C , CM000666.1:g.142728772G>C
GRCh37
NC_000004.10:g.142948222G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'