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Canonical Allele Identifier:
CA15534179
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.122995846T>C
GRCh37
chr7:g.122635900T>C
Linked Data - Sequence & Population
gnomAD v2:
7:122635900 T / C
gnomAD v3:
7:122995846 T / C
gnomAD v4:
chr7-122995846-T-C
Joint Max Group AF
0.45805865 (SAS)
Genomes Max Group AF
0.43952485 (SAS)
Exomes Max Group AF
0.45977173 (SAS)
Linked Data - NCBI & NCI
dbSNP:
978739
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.122995846T>C , CM000669.2:g.122995846T>C
GRCh38
NC_000007.13:g.122635900T>C , CM000669.1:g.122635900T>C
GRCh37
NC_000007.12:g.122423136T>C
NCBI36
NG_011980.1:g.4855A>G
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