ClinGen Allele Registry
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Canonical Allele Identifier:
CA269339732
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856393T>A
GRCh37
chr15:g.39148594T>A
Linked Data - Sequence & Population
gnomAD v2:
15:39148594 T / A
gnomAD v3:
15:38856393 T / A
gnomAD v4:
chr15-38856393-T-A
Joint Max Group AF
0.00009537 (AFR)
Genomes Max Group AF
0.00009537 (AFR)
Linked Data - NCBI & NCI
dbSNP:
560905715
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856393T>A , CM000677.2:g.38856393T>A
GRCh38
NC_000015.9:g.39148594T>A , CM000677.1:g.39148594T>A
GRCh37
NC_000015.8:g.36935886T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'