ClinGen Allele Registry
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Canonical Allele Identifier:
CA269621878
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.40904186G>A
GRCh37
chr15:g.41196384G>A
Linked Data - Sequence & Population
gnomAD v2:
15:41196384 G / A
gnomAD v3:
15:40904186 G / A
gnomAD v4:
chr15-40904186-G-A
Joint Max Group AF
0.02826852 (NFE)
Genomes Max Group AF
0.02826852 (NFE)
Linked Data - NCBI & NCI
dbSNP:
8036080
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.40904186G>A , CM000677.2:g.40904186G>A
GRCh38
NC_000015.9:g.41196384G>A , CM000677.1:g.41196384G>A
GRCh37
NC_000015.8:g.38983676G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'