ClinGen Allele Registry
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Canonical Allele Identifier:
CA13371195
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.4094257T>C
GRCh37
chr11:g.4115487T>C
Linked Data - Sequence & Population
gnomAD v2:
11:4115487 T / C
gnomAD v3:
11:4094257 T / C
gnomAD v4:
chr11-4094257-T-C
Joint Max Group AF
0.43682971 (SAS)
Genomes Max Group AF
0.43682971 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11030918
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.4094257T>C , CM000673.2:g.4094257T>C
GRCh38
NC_000011.9:g.4115487T>C , CM000673.1:g.4115487T>C
GRCh37
NC_000011.8:g.4072063T>C
NCBI36
NG_016277.1:g.243555T>C , LRG_164:g.243555T>C
NG_027992.2:g.4564T>C
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