ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11001527
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.15642347G>T
GRCh37
chr2:g.15782471G>T
Linked Data - Sequence & Population
gnomAD v2:
2:15782471 G / T
gnomAD v3:
2:15642347 G / T
gnomAD v4:
chr2-15642347-G-T
Joint Max Group AF
0.77706432 (EAS)
Genomes Max Group AF
0.77706432 (EAS)
Linked Data - NCBI & NCI
dbSNP:
807624
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.15642347G>T , CM000664.2:g.15642347G>T
GRCh38
NC_000002.11:g.15782471G>T , CM000664.1:g.15782471G>T
GRCh37
NC_000002.10:g.15699922G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'