ClinGen Allele Registry
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Canonical Allele Identifier:
CA13952068
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.104796031C>G
GRCh37
chr14:g.105262368C>G
Linked Data - Sequence & Population
gnomAD v2:
14:105262368 C / G
gnomAD v3:
14:104796031 C / G
gnomAD v4:
chr14-104796031-C-G
Joint Max Group AF
0.60537105 (NFE)
Genomes Max Group AF
0.60537105 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2498786
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.104796031C>G , CM000676.2:g.104796031C>G
GRCh38
NC_000014.8:g.105262368C>G , CM000676.1:g.105262368C>G
GRCh37
NC_000014.7:g.104333413C>G
NCBI36
NG_012188.1:g.4713G>C , LRG_721:g.4713G>C
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