ClinGen Allele Registry
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Canonical Allele Identifier:
CA640048657
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.50533323A>T
GRCh37
chr22:g.50971752A>T
Linked Data - Sequence & Population
gnomAD v2:
22:50971752 A / T
gnomAD v3:
22:50533323 A / T
gnomAD v4:
chr22-50533323-A-T
Linked Data - NCBI & NCI
dbSNP:
131794
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.50533323A>T , CM000684.2:g.50533323A>T
GRCh38
NC_000022.10:g.50971752A>T , CM000684.1:g.50971752A>T
GRCh37
NC_000022.9:g.49318618A>T
NCBI36
NG_011860.1:g.1763T>A , LRG_727:g.1763T>A
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