ClinGen Allele Registry
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Canonical Allele Identifier:
CA94290232
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.24739335G>T
GRCh37
chr4:g.24740958G>T
Linked Data - Sequence & Population
gnomAD v2:
4:24740958 G / T
gnomAD v3:
4:24739335 G / T
gnomAD v4:
chr4-24739335-G-T
Joint Max Group AF
0.15365817 (MID)
Genomes Max Group AF
0.12998794 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12500612
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.24739335G>T , CM000666.2:g.24739335G>T
GRCh38
NC_000004.11:g.24740958G>T , CM000666.1:g.24740958G>T
GRCh37
NC_000004.10:g.24350056G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'