ClinGen Allele Registry
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Canonical Allele Identifier:
CA108770458
Gene:
Linked Data
dbSNP Id:
rs1040887359
MyVariant Identifiers:
chr4:g.155515426A>T (hg19)
chr4:g.154594274A>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154594274A>T , CM000666.2:g.154594274A>T
GRCh38
NC_000004.11:g.155515426A>T , CM000666.1:g.155515426A>T
GRCh37
NC_000004.10:g.155734876A>T
NCBI36
NG_008832.1:g.1472T>A , LRG_557:g.1472T>A
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