ClinGen Allele Registry
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Canonical Allele Identifier:
CA137033192
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32691805A>G
GRCh37
chr6:g.32659582A>G
Linked Data - Sequence & Population
gnomAD v2:
6:32659582 A / G
gnomAD v3:
6:32691805 A / G
gnomAD v4:
chr6-32691805-A-G
Joint Max Group AF
0.09207804 (AMR)
Genomes Max Group AF
0.09207804 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4713586
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32691805A>G , CM000668.2:g.32691805A>G
GRCh38
NC_000006.11:g.32659582A>G , CM000668.1:g.32659582A>G
GRCh37
NC_000006.10:g.32767560A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'