ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15739478
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.65978100G>T
GRCh37
chr12:g.66371880G>T
Linked Data - Sequence & Population
gnomAD v2:
12:66371880 G / T
gnomAD v3:
12:65978100 G / T
gnomAD v4:
chr12-65978100-G-T
Joint Max Group AF
0.87842814 (EAS)
Genomes Max Group AF
0.87842814 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7968682
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.65978100G>T , CM000674.2:g.65978100G>T
GRCh38
NC_000012.11:g.66371880G>T , CM000674.1:g.66371880G>T
GRCh37
NC_000012.10:g.64658147G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'