ClinGen Allele Registry
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Canonical Allele Identifier:
CA317824436
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472606G>A
GRCh37
chr21:g.15844927G>A
Linked Data - Sequence & Population
gnomAD v3:
21:14472606 G / A
gnomAD v4:
chr21-14472606-G-A
Linked Data - NCBI & NCI
dbSNP:
986315070
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472606G>A , CM000683.2:g.14472606G>A
GRCh38
NC_000021.8:g.15844927G>A , CM000683.1:g.15844927G>A
GRCh37
NC_000021.7:g.14766798G>A
NCBI36
Search 100 bp 5'
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