ClinGen Allele Registry
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Canonical Allele Identifier:
CA574211711
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.41235906C>A
GRCh37
chr7:g.41275504C>A
Linked Data - Sequence & Population
gnomAD v2:
7:41275504 C / A
gnomAD v3:
7:41235906 C / A
gnomAD v4:
chr7-41235906-C-A
Joint Max Group AF
0.00005296 (AMR)
Genomes Max Group AF
0.00005296 (AMR)
Linked Data - NCBI & NCI
dbSNP:
12019358
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.41235906C>A , CM000669.2:g.41235906C>A
GRCh38
NC_000007.13:g.41275504C>A , CM000669.1:g.41275504C>A
GRCh37
NC_000007.12:g.41242029C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'