ClinGen Allele Registry
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Canonical Allele Identifier:
CA102264784
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.94693127C>T
GRCh37
chr4:g.95614278C>T
Linked Data - Sequence & Population
gnomAD v2:
4:95614278 C / T
gnomAD v3:
4:94693127 C / T
gnomAD v4:
chr4-94693127-C-T
Joint Max Group AF
0.30731685 (EAS)
Genomes Max Group AF
0.30731685 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17022027
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.94693127C>T , CM000666.2:g.94693127C>T
GRCh38
NC_000004.11:g.95614278C>T , CM000666.1:g.95614278C>T
GRCh37
NC_000004.10:g.95833301C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'