ClinGen Allele Registry
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Canonical Allele Identifier:
CA315645876
Gene:
Linked Data
dbSNP Id:
rs995612595
MyVariant Identifiers:
chr20:g.44742827C>G (hg19)
chr20:g.46114188C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46114188C>G , CM000682.2:g.46114188C>G
GRCh38
NC_000020.10:g.44742827C>G , CM000682.1:g.44742827C>G
GRCh37
NC_000020.9:g.44176234C>G
NCBI36
NG_007279.1:g.922C>G , LRG_40:g.922C>G
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