ClinGen Allele Registry
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Canonical Allele Identifier:
CA100014527
Gene:
Linked Data
dbSNP Id:
rs1006274309
MyVariant Identifiers:
chr4:g.81184257C>T (hg19)
chr4:g.80263103C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.80263103C>T , CM000666.2:g.80263103C>T
GRCh38
NC_000004.11:g.81184257C>T , CM000666.1:g.81184257C>T
GRCh37
NC_000004.10:g.81403281C>T
NCBI36
NG_029501.1:g.1516C>T
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