ClinGen Allele Registry
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Canonical Allele Identifier:
CA105946279
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.132405240T>C
GRCh37
chr4:g.133326395T>C
Linked Data - Sequence & Population
gnomAD v2:
4:133326395 T / C
gnomAD v3:
4:132405240 T / C
gnomAD v4:
chr4-132405240-T-C
Joint Max Group AF
0.44708205 (AMR)
Genomes Max Group AF
0.44708205 (AMR)
Linked Data - NCBI & NCI
dbSNP:
7690467
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.132405240T>C , CM000666.2:g.132405240T>C
GRCh38
NC_000004.11:g.133326395T>C , CM000666.1:g.133326395T>C
GRCh37
NC_000004.10:g.133545845T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'