ClinGen Allele Registry
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Canonical Allele Identifier:
CA11704663
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.153682710G>A
GRCh37
chr4:g.154603862G>A
Linked Data - Sequence & Population
gnomAD v2:
4:154603862 G / A
gnomAD v3:
4:153682710 G / A
gnomAD v4:
chr4-153682710-G-A
Joint Max Group AF
0.32906395 (NFE)
Genomes Max Group AF
0.32906395 (NFE)
Linked Data - NCBI & NCI
dbSNP:
76112010
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.153682710G>A , CM000666.2:g.153682710G>A
GRCh38
NC_000004.11:g.154603862G>A , CM000666.1:g.154603862G>A
GRCh37
NC_000004.10:g.154823312G>A
NCBI36
NG_016229.1:g.3422G>A
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