ClinGen Allele Registry
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Canonical Allele Identifier:
CA579559960
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.5213890T>G
GRCh37
chr8:g.5071412T>G
Linked Data - Sequence & Population
gnomAD v2:
8:5071412 T / G
gnomAD v3:
8:5213890 T / G
gnomAD v4:
chr8-5213890-T-G
Linked Data - NCBI & NCI
dbSNP:
7816936
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.5213890T>G , CM000670.2:g.5213890T>G
GRCh38
NC_000008.10:g.5071412T>G , CM000670.1:g.5071412T>G
GRCh37
NC_000008.9:g.5058820T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'