ClinGen Allele Registry
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Canonical Allele Identifier:
CA422617213
Gene:
Linked Data
dbSNP Id:
rs1366588437
MyVariant Identifiers:
chr1:g.202908763T>C (hg19)
chr1:g.202939635T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.202939635T>C , CM000663.2:g.202939635T>C
GRCh38
NC_000001.10:g.202908763T>C , CM000663.1:g.202908763T>C
GRCh37
NC_000001.9:g.201175386T>C
NCBI36
NG_052860.1:g.23938A>G
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