ClinGen Allele Registry
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Canonical Allele Identifier:
CA126566
Gene:
Linked Data
MyVariant Identifiers:
chr1:g.172627498C>C (hg19)
chr1:g.172658358C>C (hg38)
PubMed:
PMID:15937082
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.172658358C= , CM000663.2:g.172658358C=
GRCh38
NC_000001.10:g.172627498C= , CM000663.1:g.172627498C=
GRCh37
NC_000001.9:g.170894121C=
NCBI36
NG_007269.1:g.4314C= , LRG_58:g.4314C=
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