ClinGen Allele Registry
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Canonical Allele Identifier:
CA785229188
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.109878941A>T
GRCh37
chr4:g.110800097A>T
Linked Data - Sequence & Population
gnomAD v3:
4:109878941 A / T
gnomAD v4:
chr4-109878941-A-T
Linked Data - NCBI & NCI
dbSNP:
6847149
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.109878941A>T , CM000666.2:g.109878941A>T
GRCh38
NC_000004.11:g.110800097A>T , CM000666.1:g.110800097A>T
GRCh37
NC_000004.10:g.111019546A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'