ClinGen Allele Registry
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Canonical Allele Identifier:
CA32978865
Gene:
Linked Data
dbSNP Id:
rs912879228
MyVariant Identifiers:
chr1:g.172627522T>C (hg19)
chr1:g.172658382T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.172658382T>C , CM000663.2:g.172658382T>C
GRCh38
NC_000001.10:g.172627522T>C , CM000663.1:g.172627522T>C
GRCh37
NC_000001.9:g.170894145T>C
NCBI36
NG_007269.1:g.4338T>C , LRG_58:g.4338T>C
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