ClinGen Allele Registry
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Canonical Allele Identifier:
CA15538585
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.65939496G>A
GRCh37
chr8:g.66851731G>A
Linked Data - Sequence & Population
gnomAD v2:
8:66851731 G / A
gnomAD v3:
8:65939496 G / A
gnomAD v4:
chr8-65939496-G-A
Joint Max Group AF
0.73209804 (AFR)
Genomes Max Group AF
0.73209804 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4601292
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.65939496G>A , CM000670.2:g.65939496G>A
GRCh38
NC_000008.10:g.66851731G>A , CM000670.1:g.66851731G>A
GRCh37
NC_000008.9:g.67014285G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'