ClinGen Allele Registry
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Canonical Allele Identifier:
CA222541980
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.55863349C>T
GRCh37
chr11:g.55630825C>T
Linked Data - NCBI & NCI
dbSNP:
10897346
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.55863349C>T , CM000673.2:g.55863349C>T
GRCh38
NC_000011.9:g.55630825C>T , CM000673.1:g.55630825C>T
GRCh37
NC_000011.8:g.55387401C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'