ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12474137
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.82708543G>T
GRCh37
chr7:g.82337859G>T
Linked Data - Sequence & Population
gnomAD v2:
7:82337859 G / T
gnomAD v3:
7:82708543 G / T
gnomAD v4:
chr7-82708543-G-T
Joint Max Group AF
0.46878207 (AFR)
Genomes Max Group AF
0.46878207 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2371208
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.82708543G>T , CM000669.2:g.82708543G>T
GRCh38
NC_000007.13:g.82337859G>T , CM000669.1:g.82337859G>T
GRCh37
NC_000007.12:g.82175795G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'