ClinGen Allele Registry
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Canonical Allele Identifier:
CA12824099
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.142610477T>A
GRCh37
chr8:g.143691838T>A
Linked Data - Sequence & Population
gnomAD v2:
8:143691838 T / A
gnomAD v3:
8:142610477 T / A
gnomAD v4:
chr8-142610477-T-A
Joint Max Group AF
0.34257966 (MID)
Genomes Max Group AF
0.28229415 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7465272
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.142610477T>A , CM000670.2:g.142610477T>A
GRCh38
NC_000008.10:g.143691838T>A , CM000670.1:g.143691838T>A
GRCh37
NC_000008.9:g.143688840T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'