ClinGen Allele Registry
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Canonical Allele Identifier:
CA12179466
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.7106083G>C
GRCh37
chr6:g.7106316G>C
Linked Data - Sequence & Population
gnomAD v2:
6:7106316 G / C
gnomAD v3:
6:7106083 G / C
gnomAD v4:
chr6-7106083-G-C
Joint Max Group AF
0.55999234 (NFE)
Genomes Max Group AF
0.55999234 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2842895
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.7106083G>C , CM000668.2:g.7106083G>C
GRCh38
NC_000006.11:g.7106316G>C , CM000668.1:g.7106316G>C
GRCh37
NC_000006.10:g.7051315G>C
NCBI36
NG_016201.1:g.3487G>C
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