ClinGen Allele Registry
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Canonical Allele Identifier:
CA712620536
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856477G>A
GRCh37
chr15:g.39148678G>A
Linked Data - Sequence & Population
gnomAD v3:
15:38856477 G / A
gnomAD v4:
chr15-38856477-G-A
Joint Max Group AF
0.00003761 (NFE)
Genomes Max Group AF
0.00003761 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1391947865
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856477G>A , CM000677.2:g.38856477G>A
GRCh38
NC_000015.9:g.39148678G>A , CM000677.1:g.39148678G>A
GRCh37
NC_000015.8:g.36935970G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'