ClinGen Allele Registry
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Canonical Allele Identifier:
CA902378399
Gene:
Linked Data
dbSNP Id:
rs192691719
MyVariant Identifiers:
chr3:g.169482859C>G (hg19)
chr3:g.169765071C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765071C>G , CM000665.2:g.169765071C>G
GRCh38
NC_000003.11:g.169482859C>G , CM000665.1:g.169482859C>G
GRCh37
NC_000003.10:g.170965553C>G
NCBI36
NG_016363.1:g.4990G>C , LRG_347:g.4990G>C
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