ClinGen Allele Registry
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Canonical Allele Identifier:
CA32418466
Gene:
Linked Data
dbSNP Id:
rs900022735
MyVariant Identifiers:
chr1:g.169556007C>T (hg19)
chr1:g.169586769C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.169586769C>T , CM000663.2:g.169586769C>T
GRCh38
NC_000001.10:g.169556007C>T , CM000663.1:g.169556007C>T
GRCh37
NC_000001.9:g.167822631C>T
NCBI36
NG_011806.1:g.4763G>A , LRG_553:g.4763G>A
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