ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16514000
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.95598638G>A
GRCh37
chr15:g.96141867G>A
Linked Data - Sequence & Population
gnomAD v2:
15:96141867 G / A
gnomAD v3:
15:95598638 G / A
gnomAD v4:
chr15-95598638-G-A
Joint Max Group AF
0.15519815 (AFR)
Genomes Max Group AF
0.15519815 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10520789
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.95598638G>A , CM000677.2:g.95598638G>A
GRCh38
NC_000015.9:g.96141867G>A , CM000677.1:g.96141867G>A
GRCh37
NC_000015.8:g.93942871G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'