ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12440995
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29967473G>A
GRCh37
chr6:g.29935250G>A
Linked Data - Sequence & Population
gnomAD v2:
6:29935250 G / A
gnomAD v3:
6:29967473 G / A
gnomAD v4:
chr6-29967473-G-A
Joint Max Group AF
0.63014241 (SAS)
Genomes Max Group AF
0.63014241 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3893464
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29967473G>A , CM000668.2:g.29967473G>A
GRCh38
NC_000006.11:g.29935250G>A , CM000668.1:g.29935250G>A
GRCh37
NC_000006.10:g.30043229G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'