ClinGen Allele Registry
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Canonical Allele Identifier:
CA177347279
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.60963501C>A
GRCh37
chr8:g.61876060C>A
Linked Data - Sequence & Population
gnomAD v2:
8:61876060 C / A
gnomAD v3:
8:60963501 C / A
gnomAD v4:
chr8-60963501-C-A
Linked Data - NCBI & NCI
dbSNP:
932254456
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.60963501C>A , CM000670.2:g.60963501C>A
GRCh38
NC_000008.10:g.61876060C>A , CM000670.1:g.61876060C>A
GRCh37
NC_000008.9:g.62038614C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'