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Canonical Allele Identifier:
CA12766518
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.75318066G>T
GRCh37
chr8:g.76230301G>T
Linked Data - Sequence & Population
gnomAD v2:
8:76230301 G / T
gnomAD v3:
8:75318066 G / T
gnomAD v4:
chr8-75318066-G-T
Joint Max Group AF
0.94141686 (EAS)
Genomes Max Group AF
0.94141686 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6472903
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.75318066G>T , CM000670.2:g.75318066G>T
GRCh38
NC_000008.10:g.76230301G>T , CM000670.1:g.76230301G>T
GRCh37
NC_000008.9:g.76392856G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'