ClinGen Allele Registry
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Canonical Allele Identifier:
CA658655868
Gene:
Linked Data
ClinVar Variation Id:
469895
ClinVar RCV Id:
RCV003537060
dbSNP Id:
rs1554060114
MyVariant Identifiers:
chr5:g.112043062C>T (hg19)
chr5:g.112707365C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.112707365C>T , CM000667.2:g.112707365C>T
GRCh38
NC_000005.9:g.112043062C>T , CM000667.1:g.112043062C>T
GRCh37
NC_000005.8:g.112070961C>T
NCBI36
NG_008481.4:g.19845C>T , LRG_130:g.19845C>T
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