ClinGen Allele Registry
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Canonical Allele Identifier:
CA12837092
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.54414531G>A
GRCh37
chr8:g.55327091G>A
Linked Data - Sequence & Population
gnomAD v2:
8:55327091 G / A
gnomAD v3:
8:54414531 G / A
gnomAD v4:
chr8-54414531-G-A
Joint Max Group AF
0.33345083 (SAS)
Genomes Max Group AF
0.33345083 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10958409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.54414531G>A , CM000670.2:g.54414531G>A
GRCh38
NC_000008.10:g.55327091G>A , CM000670.1:g.55327091G>A
GRCh37
NC_000008.9:g.55489644G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'