ClinGen Allele Registry
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Canonical Allele Identifier:
CA13605123
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.121625105T>C
GRCh37
chr12:g.122063010T>C
Linked Data - Sequence & Population
gnomAD v2:
12:122063010 T / C
gnomAD v3:
12:121625105 T / C
gnomAD v4:
chr12-121625105-T-C
Joint Max Group AF
0.35164607 (SAS)
Genomes Max Group AF
0.35164607 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12313273
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.121625105T>C , CM000674.2:g.121625105T>C
GRCh38
NC_000012.11:g.122063010T>C , CM000674.1:g.122063010T>C
GRCh37
NC_000012.10:g.120547393T>C
NCBI36
NG_007500.1:g.3536T>C , LRG_93:g.3536T>C
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