ClinGen Allele Registry
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Canonical Allele Identifier:
CA11172134
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.219043647T>G
GRCh37
chr2:g.219908369T>G
Linked Data - Sequence & Population
gnomAD v2:
2:219908369 T / G
gnomAD v3:
2:219043647 T / G
gnomAD v4:
chr2-219043647-T-G
Joint Max Group AF
0.3814505 (AFR)
Genomes Max Group AF
0.3814505 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12470505
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.219043647T>G , CM000664.2:g.219043647T>G
GRCh38
NC_000002.11:g.219908369T>G , CM000664.1:g.219908369T>G
GRCh37
NC_000002.10:g.219616613T>G
NCBI36
NG_051336.1:g.2905A>C
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