ClinGen Allele Registry
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Canonical Allele Identifier:
CA13154218
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.49607466G>A
GRCh37
chr10:g.50815512G>A
Linked Data - Sequence & Population
gnomAD v2:
10:50815512 G / A
gnomAD v3:
10:49607466 G / A
gnomAD v4:
chr10-49607466-G-A
Joint Max Group AF
0.62343083 (NFE)
Genomes Max Group AF
0.62343083 (NFE)
Linked Data - NCBI & NCI
dbSNP:
885834
2131440356
2131440370
2131440371
2131440380
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.49607466G>A , CM000672.2:g.49607466G>A
GRCh38
NC_000010.10:g.50815512G>A , CM000672.1:g.50815512G>A
GRCh37
NC_000010.9:g.50485518G>A
NCBI36
NG_011797.1:g.3372G>A
NG_053144.1:g.2166G>A
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