ClinGen Allele Registry
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Canonical Allele Identifier:
CA32978866
Gene:
Linked Data
dbSNP Id:
rs989294188
MyVariant Identifiers:
chr1:g.172627539C>T (hg19)
chr1:g.172658399C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.172658399C>T , CM000663.2:g.172658399C>T
GRCh38
NC_000001.10:g.172627539C>T , CM000663.1:g.172627539C>T
GRCh37
NC_000001.9:g.170894162C>T
NCBI36
NG_007269.1:g.4355C>T , LRG_58:g.4355C>T
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