ClinGen Allele Registry
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Canonical Allele Identifier:
CA754066261
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.50533323A>G
GRCh37
chr22:g.50971752A>G
Linked Data - NCBI & NCI
dbSNP:
131794
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.50533323A>G , CM000684.2:g.50533323A>G
GRCh38
NC_000022.10:g.50971752A>G , CM000684.1:g.50971752A>G
GRCh37
NC_000022.9:g.49318618A>G
NCBI36
NG_011860.1:g.1763T>C , LRG_727:g.1763T>C
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