ClinGen Allele Registry
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Canonical Allele Identifier:
CA748203749
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.26171790A>C
GRCh37
chr21:g.27544108A>C
Linked Data - NCBI & NCI
dbSNP:
466448
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.26171790A>C , CM000683.2:g.26171790A>C
GRCh38
NC_000021.8:g.27544108A>C , CM000683.1:g.27544108A>C
GRCh37
NC_000021.7:g.26465979A>C
NCBI36
NG_007376.1:g.4025T>G
NG_007376.2:g.4339T>G
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