ClinGen Allele Registry
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Canonical Allele Identifier:
CA14816203
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.4717980G>T
GRCh37
chr20:g.4698626G>T
Linked Data - Sequence & Population
gnomAD v2:
20:4698626 G / T
gnomAD v3:
20:4717980 G / T
gnomAD v4:
chr20-4717980-G-T
Joint Max Group AF
0.19112797 (AFR)
Genomes Max Group AF
0.19112797 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6116492
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.4717980G>T , CM000682.2:g.4717980G>T
GRCh38
NC_000020.10:g.4698626G>T , CM000682.1:g.4698626G>T
GRCh37
NC_000020.9:g.4646626G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'