ClinGen Allele Registry
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Canonical Allele Identifier:
CA12917201
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.91406400G>A
GRCh37
chr8:g.92418628G>A
Linked Data - Sequence & Population
gnomAD v2:
8:92418628 G / A
gnomAD v3:
8:91406400 G / A
gnomAD v4:
chr8-91406400-G-A
Joint Max Group AF
0.14686129 (AFR)
Genomes Max Group AF
0.14686129 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10504906
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.91406400G>A , CM000670.2:g.91406400G>A
GRCh38
NC_000008.10:g.92418628G>A , CM000670.1:g.92418628G>A
GRCh37
NC_000008.9:g.92487804G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'