ClinGen Allele Registry
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Canonical Allele Identifier:
CA15895334
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.77948568G>A
GRCh37
chr17:g.75944650G>A
Linked Data - Sequence & Population
gnomAD v2:
17:75944650 G / A
gnomAD v3:
17:77948568 G / A
gnomAD v4:
chr17-77948568-G-A
Joint Max Group AF
0.39828684 (EAS)
Genomes Max Group AF
0.39828684 (EAS)
Linked Data - NCBI & NCI
dbSNP:
16970672
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.77948568G>A , CM000679.2:g.77948568G>A
GRCh38
NC_000017.10:g.75944650G>A , CM000679.1:g.75944650G>A
GRCh37
NC_000017.9:g.73456245G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'