ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12630696
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.35515178C>T
GRCh37
chr7:g.35554788C>T
Linked Data - Sequence & Population
gnomAD v2:
7:35554788 C / T
gnomAD v3:
7:35515178 C / T
gnomAD v4:
chr7-35515178-C-T
Joint Max Group AF
0.46657124 (EAS)
Genomes Max Group AF
0.46657124 (EAS)
Linked Data - NCBI & NCI
dbSNP:
343064
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.35515178C>T , CM000669.2:g.35515178C>T
GRCh38
NC_000007.13:g.35554788C>T , CM000669.1:g.35554788C>T
GRCh37
NC_000007.12:g.35521313C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'