ClinGen Allele Registry
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Canonical Allele Identifier:
CA12441321
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31462150T>C
GRCh37
chr6:g.31429927T>C
Linked Data - Sequence & Population
gnomAD v2:
6:31429927 T / C
gnomAD v3:
6:31462150 T / C
gnomAD v4:
chr6-31462150-T-C
Joint Max Group AF
0.28550135 (SAS)
Genomes Max Group AF
0.28550135 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3094228
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31462150T>C , CM000668.2:g.31462150T>C
GRCh38
NC_000006.11:g.31429927T>C , CM000668.1:g.31429927T>C
GRCh37
NC_000006.10:g.31537906T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'