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Canonical Allele Identifier:
CA13649118
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.67643308G>T
GRCh37
chr12:g.68037088G>T
Linked Data - Sequence & Population
gnomAD v2:
12:68037088 G / T
gnomAD v3:
12:67643308 G / T
gnomAD v4:
chr12-67643308-G-T
Joint Max Group AF
0.3562724 (AMR)
Genomes Max Group AF
0.3562724 (AMR)
Linked Data - NCBI & NCI
dbSNP:
10878640
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.67643308G>T , CM000674.2:g.67643308G>T
GRCh38
NC_000012.11:g.68037088G>T , CM000674.1:g.68037088G>T
GRCh37
NC_000012.10:g.66323355G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'