ClinGen Allele Registry
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Canonical Allele Identifier:
CA138024553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.41287773A>G
GRCh37
chr6:g.41255511A>G
Linked Data - Sequence & Population
gnomAD v2:
6:41255511 A / G
gnomAD v3:
6:41287773 A / G
gnomAD v4:
chr6-41287773-A-G
Joint Max Group AF
0.88218957 (AFR)
Genomes Max Group AF
0.88218957 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7768162
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.41287773A>G , CM000668.2:g.41287773A>G
GRCh38
NC_000006.11:g.41255511A>G , CM000668.1:g.41255511A>G
GRCh37
NC_000006.10:g.41363489A>G
NCBI36
NG_029525.1:g.3947T>C
NG_029525.2:g.3947T>C
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