ClinGen Allele Registry
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Canonical Allele Identifier:
CA106792469
Gene:
Linked Data
dbSNP Id:
rs1023002969
MyVariant Identifiers:
chr4:g.141493930T>C (hg19)
chr4:g.140572776T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.140572776T>C , CM000666.2:g.140572776T>C
GRCh38
NC_000004.11:g.141493930T>C , CM000666.1:g.141493930T>C
GRCh37
NC_000004.10:g.141713380T>C
NCBI36
NG_012139.1:g.1030A>G
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