ClinGen Allele Registry
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Canonical Allele Identifier:
CA63790285
Gene:
Linked Data
dbSNP Id:
rs575869629
MyVariant Identifiers:
chr2:g.204738984C>T (hg19)
chr2:g.203874261C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874261C>T , CM000664.2:g.203874261C>T
GRCh38
NC_000002.11:g.204738984C>T , CM000664.1:g.204738984C>T
GRCh37
NC_000002.10:g.204447229C>T
NCBI36
NG_011502.1:g.11476C>T
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