ClinGen Allele Registry
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Canonical Allele Identifier:
CA269339726
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856348G>A
GRCh37
chr15:g.39148549G>A
Linked Data - Sequence & Population
gnomAD v2:
15:39148549 G / A
gnomAD v3:
15:38856348 G / A
gnomAD v4:
chr15-38856348-G-A
Joint Max Group AF
0.00271288 (AFR)
Genomes Max Group AF
0.00271288 (AFR)
Linked Data - NCBI & NCI
dbSNP:
73396144
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856348G>A , CM000677.2:g.38856348G>A
GRCh38
NC_000015.9:g.39148549G>A , CM000677.1:g.39148549G>A
GRCh37
NC_000015.8:g.36935841G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'