ClinGen Allele Registry
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Canonical Allele Identifier:
CA119694880
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.57876251T>C
GRCh37
chr5:g.57172078T>C
Linked Data - Sequence & Population
gnomAD v2:
5:57172078 T / C
gnomAD v3:
5:57876251 T / C
gnomAD v4:
chr5-57876251-T-C
Joint Max Group AF
0.73688126 (AFR)
Genomes Max Group AF
0.73688126 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4432842
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.57876251T>C , CM000667.2:g.57876251T>C
GRCh38
NC_000005.9:g.57172078T>C , CM000667.1:g.57172078T>C
GRCh37
NC_000005.8:g.57207835T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'