ClinGen Allele Registry
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Canonical Allele Identifier:
CA12335612
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.132572573G>A
GRCh37
chr6:g.132893712G>A
Linked Data - Sequence & Population
gnomAD v2:
6:132893712 G / A
gnomAD v3:
6:132572573 G / A
gnomAD v4:
chr6-132572573-G-A
Joint Max Group AF
0.60623904 (SAS)
Genomes Max Group AF
0.60623904 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4305745
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.132572573G>A , CM000668.2:g.132572573G>A
GRCh38
NC_000006.11:g.132893712G>A , CM000668.1:g.132893712G>A
GRCh37
NC_000006.10:g.132935405G>A
NCBI36
NG_016544.1:g.7252G>A
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