ClinGen Allele Registry
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Canonical Allele Identifier:
CA12188767
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32892975G>A
GRCh37
chr6:g.32860752G>A
Linked Data - Sequence & Population
gnomAD v2:
6:32860752 G / A
gnomAD v3:
6:32892975 G / A
gnomAD v4:
chr6-32892975-G-A
Joint Max Group AF
0.18994124 (AFR)
Genomes Max Group AF
0.18994124 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9469300
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32892975G>A , CM000668.2:g.32892975G>A
GRCh38
NC_000006.11:g.32860752G>A , CM000668.1:g.32860752G>A
GRCh37
NC_000006.10:g.32968730G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'