ClinGen Allele Registry
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Canonical Allele Identifier:
CA13605122
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.121624817G>T
GRCh37
chr12:g.122062722G>T
Linked Data - Sequence & Population
gnomAD v2:
12:122062722 G / T
gnomAD v3:
12:121624817 G / T
gnomAD v4:
chr12-121624817-G-T
Joint Max Group AF
0.68260339 (AFR)
Genomes Max Group AF
0.68260339 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12320939
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.121624817G>T , CM000674.2:g.121624817G>T
GRCh38
NC_000012.11:g.122062722G>T , CM000674.1:g.122062722G>T
GRCh37
NC_000012.10:g.120547105G>T
NCBI36
NG_007500.1:g.3248G>T , LRG_93:g.3248G>T
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