ClinGen Allele Registry
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Canonical Allele Identifier:
CA12476909
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.100899511A>G
GRCh37
chr7:g.100497131A>G
Linked Data - Sequence & Population
gnomAD v2:
7:100497131 A / G
gnomAD v3:
7:100899511 A / G
gnomAD v4:
chr7-100899511-A-G
Joint Max Group AF
0.37578205 (EAS)
Genomes Max Group AF
0.37578205 (EAS)
Linked Data - NCBI & NCI
dbSNP:
13245899
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.100899511A>G , CM000669.2:g.100899511A>G
GRCh38
NC_000007.13:g.100497131A>G , CM000669.1:g.100497131A>G
GRCh37
NC_000007.12:g.100335067A>G
NCBI36
NG_007474.1:g.1411T>C
NG_007474.2:g.1623T>C
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