ClinGen Allele Registry
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Canonical Allele Identifier:
CA15082745
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.202959575G>A
GRCh37
chr1:g.202928703G>A
Linked Data - Sequence & Population
gnomAD v2:
1:202928703 G / A
gnomAD v3:
1:202959575 G / A
gnomAD v4:
chr1-202959575-G-A
Joint Max Group AF
0.29560754 (NFE)
Genomes Max Group AF
0.29560754 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6666089
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.202959575G>A , CM000663.2:g.202959575G>A
GRCh38
NC_000001.10:g.202928703G>A , CM000663.1:g.202928703G>A
GRCh37
NC_000001.9:g.201195326G>A
NCBI36
NG_052860.1:g.3998C>T
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