ClinGen Allele Registry
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Canonical Allele Identifier:
CA12305739
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.131953590G>A
GRCh37
chr6:g.132274730G>A
Linked Data - Sequence & Population
gnomAD v2:
6:132274730 G / A
gnomAD v3:
6:131953590 G / A
gnomAD v4:
chr6-131953590-G-A
Joint Max Group AF
0.89384932 (NFE)
Genomes Max Group AF
0.89384932 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2151532
2113356203
2113356208
2113356214
2113356223
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.131953590G>A , CM000668.2:g.131953590G>A
GRCh38
NC_000006.11:g.132274730G>A , CM000668.1:g.132274730G>A
GRCh37
NC_000006.10:g.132316423G>A
NCBI36
NG_016131.1:g.2789C>T
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