ClinGen Allele Registry
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Canonical Allele Identifier:
CA12745545
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.143611669C>T
GRCh37
chr8:g.144693839C>T
Linked Data - Sequence & Population
gnomAD v2:
8:144693839 C / T
gnomAD v3:
8:143611669 C / T
gnomAD v4:
chr8-143611669-C-T
Joint Max Group AF
0.60509609 (NFE)
Genomes Max Group AF
0.60509609 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2045084
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.143611669C>T , CM000670.2:g.143611669C>T
GRCh38
NC_000008.10:g.144693839C>T , CM000670.1:g.144693839C>T
GRCh37
NC_000008.9:g.144764982C>T
NCBI36
NG_051357.1:g.2946G>A
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