ClinGen Allele Registry
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Canonical Allele Identifier:
CA763418001
Gene:
Linked Data
dbSNP Id:
rs1398556883
MyVariant Identifiers:
chr2:g.203240916C>G (hg19)
chr2:g.202376193C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.202376193C>G , CM000664.2:g.202376193C>G
GRCh38
NC_000002.11:g.203240916C>G , CM000664.1:g.203240916C>G
GRCh37
NC_000002.10:g.202949161C>G
NCBI36
NG_009363.1:g.4867C>G , LRG_712:g.4867C>G
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