ClinGen Allele Registry
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Canonical Allele Identifier:
CA14079209
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.46564730A>C
GRCh37
chr15:g.46856928A>C
Linked Data - Sequence & Population
gnomAD v2:
15:46856928 A / C
gnomAD v3:
15:46564730 A / C
gnomAD v4:
chr15-46564730-A-C
Joint Max Group AF
0.41166986 (AFR)
Genomes Max Group AF
0.41166986 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4775602
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.46564730A>C , CM000677.2:g.46564730A>C
GRCh38
NC_000015.9:g.46856928A>C , CM000677.1:g.46856928A>C
GRCh37
NC_000015.8:g.44644220A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'