ClinGen Allele Registry
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Canonical Allele Identifier:
CA146808600
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.121435182A>C
GRCh37
chr6:g.121756328A>C
Linked Data - Sequence & Population
gnomAD v2:
6:121756328 A / C
gnomAD v3:
6:121435182 A / C
gnomAD v4:
chr6-121435182-A-C
Joint Max Group AF
0.20421126 (EAS)
Genomes Max Group AF
0.20421126 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2071166
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.121435182A>C , CM000668.2:g.121435182A>C
GRCh38
NC_000006.11:g.121756328A>C , CM000668.1:g.121756328A>C
GRCh37
NC_000006.10:g.121798027A>C
NCBI36
NG_008308.1:g.4584A>C
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