ClinGen Allele Registry
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Canonical Allele Identifier:
CA35603485
Gene:
Linked Data
dbSNP Id:
rs369097851
MyVariant Identifiers:
chr1:g.202908863A>T (hg19)
chr1:g.202939735A>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.202939735A>T , CM000663.2:g.202939735A>T
GRCh38
NC_000001.10:g.202908863A>T , CM000663.1:g.202908863A>T
GRCh37
NC_000001.9:g.201175486A>T
NCBI36
NG_052860.1:g.23838T>A
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