ClinGen Allele Registry
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Canonical Allele Identifier:
CA13851373
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.101417809T>A
GRCh37
chr13:g.102070160T>A
Linked Data - Sequence & Population
gnomAD v2:
13:102070160 T / A
gnomAD v3:
13:101417809 T / A
gnomAD v4:
chr13-101417809-T-A
Joint Max Group AF
0.9181559 (AFR)
Genomes Max Group AF
0.9181559 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2152324
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.101417809T>A , CM000675.2:g.101417809T>A
GRCh38
NC_000013.10:g.102070160T>A , CM000675.1:g.102070160T>A
GRCh37
NC_000013.9:g.100868161T>A
NCBI36
NG_053176.1:g.4398A>T
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