ClinGen Allele Registry
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Canonical Allele Identifier:
CA13719711
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.6199357C>T
GRCh37
chr12:g.6308523C>T
Linked Data - Sequence & Population
gnomAD v2:
12:6308523 C / T
gnomAD v3:
12:6199357 C / T
gnomAD v4:
chr12-6199357-C-T
Joint Max Group AF
0.38801137 (AFR)
Genomes Max Group AF
0.38801137 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3181157
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.6199357C>T , CM000674.2:g.6199357C>T
GRCh38
NC_000012.11:g.6308523C>T , CM000674.1:g.6308523C>T
GRCh37
NC_000012.10:g.6178784C>T
NCBI36
NG_055677.1:g.4651C>T
Search 100 bp 5'
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