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Canonical Allele Identifier:
CA156347835
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.27295942T>G
GRCh37
chr7:g.27335561T>G
Linked Data - Sequence & Population
gnomAD v2:
7:27335561 T / G
gnomAD v3:
7:27295942 T / G
gnomAD v4:
chr7-27295942-T-G
Joint Max Group AF
0.09461614 (AFR)
Genomes Max Group AF
0.09461614 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11564024
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.27295942T>G , CM000669.2:g.27295942T>G
GRCh38
NC_000007.13:g.27335561T>G , CM000669.1:g.27335561T>G
GRCh37
NC_000007.12:g.27302086T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'