ClinGen Allele Registry
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Canonical Allele Identifier:
CA228623305
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113407973C>A
GRCh37
chr11:g.113278695C>A
Linked Data - Sequence & Population
gnomAD v2:
11:113278695 C / A
gnomAD v3:
11:113407973 C / A
gnomAD v4:
chr11-113407973-C-A
Joint Max Group AF
0.00003249 (AFR)
Genomes Max Group AF
0.00003249 (AFR)
Linked Data - NCBI & NCI
dbSNP:
972414814
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113407973C>A , CM000673.2:g.113407973C>A
GRCh38
NC_000011.9:g.113278695C>A , CM000673.1:g.113278695C>A
GRCh37
NC_000011.8:g.112783905C>A
NCBI36
NG_008841.1:g.72307G>T
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