ClinGen Allele Registry
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Canonical Allele Identifier:
CA256493490
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545932C>G
GRCh37
chr13:g.106198281C>G
Linked Data - NCBI & NCI
dbSNP:
1054718777
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545932C>G , CM000675.2:g.105545932C>G
GRCh38
NC_000013.10:g.106198281C>G , CM000675.1:g.106198281C>G
GRCh37
NC_000013.9:g.104996282C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'