ClinGen Allele Registry
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Canonical Allele Identifier:
CA135935716
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.28662914G>A
GRCh37
chr6:g.28630691G>A
Linked Data - Sequence & Population
gnomAD v2:
6:28630691 G / A
gnomAD v3:
6:28662914 G / A
gnomAD v4:
chr6-28662914-G-A
Joint Max Group AF
0.08691667 (NFE)
Genomes Max Group AF
0.08691667 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13194504
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.28662914G>A , CM000668.2:g.28662914G>A
GRCh38
NC_000006.11:g.28630691G>A , CM000668.1:g.28630691G>A
GRCh37
NC_000006.10:g.28738670G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'