ClinGen Allele Registry
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Canonical Allele Identifier:
CA15692822
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2163618G>T
GRCh37
chr11:g.2184848G>T
Linked Data - Sequence & Population
gnomAD v2:
11:2184848 G / T
gnomAD v3:
11:2163618 G / T
gnomAD v4:
chr11-2163618-G-T
Joint Max Group AF
0.93262277 (EAS)
Genomes Max Group AF
0.93262277 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3842727
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2163618G>T , CM000673.2:g.2163618G>T
GRCh38
NC_000011.9:g.2184848G>T , CM000673.1:g.2184848G>T
GRCh37
NC_000011.8:g.2141424G>T
NCBI36
NG_007114.1:g.2577C>A
NG_008128.1:g.13188C>A
NG_050578.1:g.2592C>A
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