ClinGen Allele Registry
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Canonical Allele Identifier:
CA262598329
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.73136378C>G
GRCh37
chr14:g.73603086C>G
Linked Data - Sequence & Population
gnomAD v2:
14:73603086 C / G
gnomAD v3:
14:73136378 C / G
gnomAD v4:
chr14-73136378-C-G
Joint Max Group AF
0.00395097 (AFR)
Genomes Max Group AF
0.00395135 (AFR)
Linked Data - NCBI & NCI
dbSNP:
530970418
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.73136378C>G , CM000676.2:g.73136378C>G
GRCh38
NC_000014.8:g.73603086C>G , CM000676.1:g.73603086C>G
GRCh37
NC_000014.7:g.72672839C>G
NCBI36
NG_007386.2:g.4908C>G
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