ClinGen Allele Registry
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Canonical Allele Identifier:
CA108694080
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.153683816A>G
GRCh37
chr4:g.154604968A>G
Linked Data - Sequence & Population
gnomAD v2:
4:154604968 A / G
gnomAD v3:
4:153683816 A / G
gnomAD v4:
chr4-153683816-A-G
Joint Max Group AF
0.98857322 (NFE)
Genomes Max Group AF
0.98857322 (NFE)
Linked Data - NCBI & NCI
dbSNP:
893629
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.153683816A>G , CM000666.2:g.153683816A>G
GRCh38
NC_000004.11:g.154604968A>G , CM000666.1:g.154604968A>G
GRCh37
NC_000004.10:g.154824418A>G
NCBI36
NG_016229.1:g.4528A>G
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