ClinGen Allele Registry
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Canonical Allele Identifier:
CA13236489
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.9007290C>T
GRCh37
chr10:g.9049253C>T
Linked Data - Sequence & Population
gnomAD v2:
10:9049253 C / T
gnomAD v3:
10:9007290 C / T
gnomAD v4:
chr10-9007290-C-T
Joint Max Group AF
0.10011046 (NFE)
Genomes Max Group AF
0.10011046 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12413578
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.9007290C>T , CM000672.2:g.9007290C>T
GRCh38
NC_000010.10:g.9049253C>T , CM000672.1:g.9049253C>T
GRCh37
NC_000010.9:g.9089259C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_930641.1:n.32+58073G>A
Search 100 bp 5'
Search 100 bp 3'