ClinGen Allele Registry
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Canonical Allele Identifier:
CA748815041
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.33395791A>T
GRCh37
chr21:g.34768097A>T
Linked Data - NCBI & NCI
dbSNP:
9976971
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.33395791A>T , CM000683.2:g.33395791A>T
GRCh38
NC_000021.8:g.34768097A>T , CM000683.1:g.34768097A>T
GRCh37
NC_000021.7:g.33689967A>T
NCBI36
NG_007570.2:g.15799A>T , LRG_67:g.15799A>T
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