ClinGen Allele Registry
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Canonical Allele Identifier:
CA15117822
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.101472921G>A
GRCh37
chr1:g.101938477G>A
Linked Data - Sequence & Population
gnomAD v2:
1:101938477 G / A
gnomAD v3:
1:101472921 G / A
gnomAD v4:
chr1-101472921-G-A
Joint Max Group AF
0.60267935 (AFR)
Genomes Max Group AF
0.60267935 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1948368
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.101472921G>A , CM000663.2:g.101472921G>A
GRCh38
NC_000001.10:g.101938477G>A , CM000663.1:g.101938477G>A
GRCh37
NC_000001.9:g.101711065G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'