ClinGen Allele Registry
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Canonical Allele Identifier:
CA11865845
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.109911150T>C
GRCh37
chr4:g.110832306T>C
Linked Data - Sequence & Population
gnomAD v2:
4:110832306 T / C
gnomAD v3:
4:109911150 T / C
gnomAD v4:
chr4-109911150-T-C
Joint Max Group AF
0.19206818 (EAS)
Genomes Max Group AF
0.19206818 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3756261
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.109911150T>C , CM000666.2:g.109911150T>C
GRCh38
NC_000004.11:g.110832306T>C , CM000666.1:g.110832306T>C
GRCh37
NC_000004.10:g.111051755T>C
NCBI36
NG_011441.1:g.3267T>C
NG_011441.2:g.3267T>C
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