ClinGen Allele Registry
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Canonical Allele Identifier:
CA31677589
Gene:
Linked Data
dbSNP Id:
rs1056614372
MyVariant Identifiers:
chr1:g.161184681A>T (hg19)
chr1:g.161214891A>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161214891A>T , CM000663.2:g.161214891A>T
GRCh38
NC_000001.10:g.161184681A>T , CM000663.1:g.161184681A>T
GRCh37
NC_000001.9:g.159451305A>T
NCBI36
NG_013352.1:g.20577A>T
NG_029043.1:g.4595A>T
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