ClinGen Allele Registry
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Canonical Allele Identifier:
CA290814667
Gene:
Linked Data
dbSNP Id:
rs970515111
MyVariant Identifiers:
chr17:g.41195523C>A (hg19)
chr17:g.43043506C>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.43043506C>A , CM000679.2:g.43043506C>A
GRCh38
NC_000017.10:g.41195523C>A , CM000679.1:g.41195523C>A
GRCh37
NC_000017.9:g.38449049C>A
NCBI36
NG_005905.2:g.174478G>T , LRG_292:g.174478G>T
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