ClinGen Allele Registry
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Canonical Allele Identifier:
CA749293194
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.39808149A>T
GRCh37
chr21:g.41180076A>T
Linked Data - NCBI & NCI
dbSNP:
2410182
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.39808149A>T , CM000683.2:g.39808149A>T
GRCh38
NC_000021.8:g.41180076A>T , CM000683.1:g.41180076A>T
GRCh37
NC_000021.7:g.40101946A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'