ClinGen Allele Registry
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Canonical Allele Identifier:
CA308507865
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.41096565A>G
GRCh37
chr19:g.41602470A>G
Linked Data - Sequence & Population
gnomAD v2:
19:41602470 A / G
gnomAD v3:
19:41096565 A / G
gnomAD v4:
chr19-41096565-A-G
Joint Max Group AF
0.20348904 (AFR)
Genomes Max Group AF
0.20348904 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1709084
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.41096565A>G , CM000681.2:g.41096565A>G
GRCh38
NC_000019.9:g.41602470A>G , CM000681.1:g.41602470A>G
GRCh37
NC_000019.8:g.46294310A>G
NCBI36
NG_007928.1:g.13103A>G
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