ClinGen Allele Registry
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Canonical Allele Identifier:
CA13578562
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.6343302C>G
GRCh37
chr12:g.6452468C>G
Linked Data - Sequence & Population
gnomAD v2:
12:6452468 C / G
gnomAD v3:
12:6343302 C / G
gnomAD v4:
chr12-6343302-C-G
Joint Max Group AF
0.42785298 (NFE)
Genomes Max Group AF
0.42785298 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4149569
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.6343302C>G , CM000674.2:g.6343302C>G
GRCh38
NC_000012.11:g.6452468C>G , CM000674.1:g.6452468C>G
GRCh37
NC_000012.10:g.6322729C>G
NCBI36
NG_007506.1:g.3794G>C , LRG_193:g.3794G>C
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