ClinGen Allele Registry
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Canonical Allele Identifier:
CA113421775
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.3416258T>C
GRCh37
chr5:g.3416372T>C
Linked Data - Sequence & Population
gnomAD v2:
5:3416372 T / C
gnomAD v3:
5:3416258 T / C
gnomAD v4:
chr5-3416258-T-C
Joint Max Group AF
0.00006284 (AFR)
Genomes Max Group AF
0.00006284 (AFR)
Linked Data - NCBI & NCI
dbSNP:
17683231
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.3416258T>C , CM000667.2:g.3416258T>C
GRCh38
NC_000005.9:g.3416372T>C , CM000667.1:g.3416372T>C
GRCh37
NC_000005.8:g.3469372T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'