ClinGen Allele Registry
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Canonical Allele Identifier:
CA13263879
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.34998722T>G
GRCh37
chr10:g.35287650T>G
Linked Data - Sequence & Population
gnomAD v2:
10:35287650 T / G
gnomAD v3:
10:34998722 T / G
gnomAD v4:
chr10-34998722-T-G
Joint Max Group AF
0.34262708 (NFE)
Genomes Max Group AF
0.34262708 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17582416
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.34998722T>G , CM000672.2:g.34998722T>G
GRCh38
NC_000010.10:g.35287650T>G , CM000672.1:g.35287650T>G
GRCh37
NC_000010.9:g.35327656T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_930817.1:n.509-4360A>C
Search 100 bp 5'
Search 100 bp 3'