ClinGen Allele Registry
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Canonical Allele Identifier:
CA12335526
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.131952851G>C
GRCh37
chr6:g.132273991G>C
Linked Data - Sequence & Population
gnomAD v2:
6:132273991 G / C
gnomAD v3:
6:131952851 G / C
gnomAD v4:
chr6-131952851-G-C
Joint Max Group AF
0.37693747 (AFR)
Genomes Max Group AF
0.37693747 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9493150
2113429935
2113429943
2113429958
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.131952851G>C , CM000668.2:g.131952851G>C
GRCh38
NC_000006.11:g.132273991G>C , CM000668.1:g.132273991G>C
GRCh37
NC_000006.10:g.132315684G>C
NCBI36
NG_016131.1:g.3528C>G
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