ClinGen Allele Registry
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Canonical Allele Identifier:
CA674610404
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2179933T>A
GRCh37
chr11:g.2201163T>A
Linked Data - Sequence & Population
gnomAD v3:
11:2179933 T / A
gnomAD v4:
chr11-2179933-T-A
Linked Data - NCBI & NCI
dbSNP:
6578993
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2179933T>A , CM000673.2:g.2179933T>A
GRCh38
NC_000011.9:g.2201163T>A , CM000673.1:g.2201163T>A
GRCh37
NC_000011.8:g.2157739T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'