ClinGen Allele Registry
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Canonical Allele Identifier:
CA269339743
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856465T>C
GRCh37
chr15:g.39148666T>C
Linked Data - Sequence & Population
gnomAD v3:
15:38856465 T / C
gnomAD v4:
chr15-38856465-T-C
Joint Max Group AF
0.00001171 (NFE)
Genomes Max Group AF
0.00001171 (NFE)
Linked Data - NCBI & NCI
dbSNP:
997652057
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856465T>C , CM000677.2:g.38856465T>C
GRCh38
NC_000015.9:g.39148666T>C , CM000677.1:g.39148666T>C
GRCh37
NC_000015.8:g.36935958T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'