ClinGen Allele Registry
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Canonical Allele Identifier:
CA12214828
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.156547814G>A
GRCh37
chr6:g.156868948G>A
Linked Data - Sequence & Population
gnomAD v2:
6:156868948 G / A
gnomAD v3:
6:156547814 G / A
gnomAD v4:
chr6-156547814-G-A
Joint Max Group AF
0.17250977 (AFR)
Genomes Max Group AF
0.17250977 (AFR)
Linked Data - NCBI & NCI
dbSNP:
502281
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.156547814G>A , CM000668.2:g.156547814G>A
GRCh38
NC_000006.11:g.156868948G>A , CM000668.1:g.156868948G>A
GRCh37
NC_000006.10:g.156910640G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'