ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13591917
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.65723778G>A
GRCh37
chr12:g.66117558G>A
Linked Data - Sequence & Population
gnomAD v2:
12:66117558 G / A
gnomAD v3:
12:65723778 G / A
gnomAD v4:
chr12-65723778-G-A
Joint Max Group AF
0.85834351 (NFE)
Genomes Max Group AF
0.85834351 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2358944
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.65723778G>A , CM000674.2:g.65723778G>A
GRCh38
NC_000012.11:g.66117558G>A , CM000674.1:g.66117558G>A
GRCh37
NC_000012.10:g.64403825G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'