ClinGen Allele Registry
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Canonical Allele Identifier:
CA748789466
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.33316948A>T
GRCh37
chr21:g.34689253A>T
Linked Data - Sequence & Population
gnomAD v3:
21:33316948 A / T
gnomAD v4:
chr21-33316948-A-T
Linked Data - NCBI & NCI
dbSNP:
2834188
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.33316948A>T , CM000683.2:g.33316948A>T
GRCh38
NC_000021.8:g.34689253A>T , CM000683.1:g.34689253A>T
GRCh37
NC_000021.7:g.33611123A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'