ClinGen Allele Registry
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Canonical Allele Identifier:
CA15436172
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32614658G>A
GRCh37
chr6:g.32582435G>A
Linked Data - Sequence & Population
gnomAD v2:
6:32582435 G / A
gnomAD v3:
6:32614658 G / A
gnomAD v4:
chr6-32614658-G-A
Joint Max Group AF
0.54660234 (MID)
Genomes Max Group AF
0.4915448 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7451962
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32614658G>A , CM000668.2:g.32614658G>A
GRCh38
NC_000006.11:g.32582435G>A , CM000668.1:g.32582435G>A
GRCh37
NC_000006.10:g.32690413G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'