ClinGen Allele Registry
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Canonical Allele Identifier:
CA15639928
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.3625534A>G
GRCh37
chr10:g.3667726A>G
Linked Data - Sequence & Population
gnomAD v2:
10:3667726 A / G
gnomAD v3:
10:3625534 A / G
gnomAD v4:
chr10-3625534-A-G
Joint Max Group AF
0.37676812 (NFE)
Genomes Max Group AF
0.37676812 (NFE)
Linked Data - NCBI & NCI
dbSNP:
705471
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.3625534A>G , CM000672.2:g.3625534A>G
GRCh38
NC_000010.10:g.3667726A>G , CM000672.1:g.3667726A>G
GRCh37
NC_000010.9:g.3657726A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_131187.1:n.163-123154A>G
Search 100 bp 5'
Search 100 bp 3'