ClinGen Allele Registry
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Canonical Allele Identifier:
CA99607192
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.81244636T>C
GRCh37
chr4:g.82165790T>C
Linked Data - Sequence & Population
gnomAD v2:
4:82165790 T / C
gnomAD v3:
4:81244636 T / C
gnomAD v4:
chr4-81244636-T-C
Joint Max Group AF
0.70953761 (AFR)
Genomes Max Group AF
0.70953761 (AFR)
Linked Data - NCBI & NCI
dbSNP:
994014
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.81244636T>C , CM000666.2:g.81244636T>C
GRCh38
NC_000004.11:g.82165790T>C , CM000666.1:g.82165790T>C
GRCh37
NC_000004.10:g.82384814T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'