ClinGen Allele Registry
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Canonical Allele Identifier:
CA12377707
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.131956291C>G
GRCh37
chr6:g.132277431C>G
Linked Data - Sequence & Population
gnomAD v2:
6:132277431 C / G
gnomAD v3:
6:131956291 C / G
gnomAD v4:
chr6-131956291-C-G
Joint Max Group AF
0.39080519 (EAS)
Genomes Max Group AF
0.39080519 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9402373
2113356249
2113356252
2113356254
2113356263
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.131956291C>G , CM000668.2:g.131956291C>G
GRCh38
NC_000006.11:g.132277431C>G , CM000668.1:g.132277431C>G
GRCh37
NC_000006.10:g.132319124C>G
NCBI36
NG_016131.1:g.88G>C
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