ClinGen Allele Registry
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Canonical Allele Identifier:
CA14098020
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.36021764G>T
GRCh37
chr15:g.36313965G>T
Linked Data - Sequence & Population
gnomAD v2:
15:36313965 G / T
gnomAD v3:
15:36021764 G / T
gnomAD v4:
chr15-36021764-G-T
Joint Max Group AF
0.31044042 (SAS)
Genomes Max Group AF
0.31044042 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10520045
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.36021764G>T , CM000677.2:g.36021764G>T
GRCh38
NC_000015.9:g.36313965G>T , CM000677.1:g.36313965G>T
GRCh37
NC_000015.8:g.34101257G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'