ClinGen Allele Registry
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Canonical Allele Identifier:
CA112146188
Gene:
Linked Data
dbSNP Id:
rs933506769
MyVariant Identifiers:
chr4:g.187187092T>G (hg19)
chr4:g.186265938T>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.186265938T>G , CM000666.2:g.186265938T>G
GRCh38
NC_000004.11:g.187187092T>G , CM000666.1:g.187187092T>G
GRCh37
NC_000004.10:g.187424086T>G
NCBI36
NG_008051.1:g.4975T>G , LRG_583:g.4975T>G
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