ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12230622
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31188008G>C
GRCh37
chr6:g.31155785G>C
Linked Data - Sequence & Population
gnomAD v2:
6:31155785 G / C
gnomAD v3:
6:31188008 G / C
gnomAD v4:
chr6-31188008-G-C
Joint Max Group AF
0.20766132 (NFE)
Genomes Max Group AF
0.20766132 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1265181
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31188008G>C , CM000668.2:g.31188008G>C
GRCh38
NC_000006.11:g.31155785G>C , CM000668.1:g.31155785G>C
GRCh37
NC_000006.10:g.31263764G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'