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Canonical Allele Identifier:
CA15527242
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.106771412T>C
GRCh37
chr7:g.106411858T>C
Linked Data - Sequence & Population
gnomAD v2:
7:106411858 T / C
gnomAD v3:
7:106771412 T / C
gnomAD v4:
chr7-106771412-T-C
Joint Max Group AF
0.28621567 (SAS)
Genomes Max Group AF
0.28621567 (SAS)
Linked Data - NCBI & NCI
dbSNP:
17477177
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.106771412T>C , CM000669.2:g.106771412T>C
GRCh38
NC_000007.13:g.106411858T>C , CM000669.1:g.106411858T>C
GRCh37
NC_000007.12:g.106199094T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'