ClinGen Allele Registry
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Canonical Allele Identifier:
CA138024550
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.41287752T>C
GRCh37
chr6:g.41255490T>C
Linked Data - Sequence & Population
gnomAD v2:
6:41255490 T / C
gnomAD v3:
6:41287752 T / C
gnomAD v4:
chr6-41287752-T-C
Joint Max Group AF
0.29349036 (EAS)
Genomes Max Group AF
0.29349036 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9471535
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.41287752T>C , CM000668.2:g.41287752T>C
GRCh38
NC_000006.11:g.41255490T>C , CM000668.1:g.41255490T>C
GRCh37
NC_000006.10:g.41363468T>C
NCBI36
NG_029525.1:g.3968A>G
NG_029525.2:g.3968A>G
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