ClinGen Allele Registry
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Canonical Allele Identifier:
CA16229545
Gene:
Linked Data
ClinVar Variation Id:
1252728
ClinVar RCV Id:
RCV001661025
dbSNP Id:
rs10042486
gnomAD v2:
5-63261329-C-T
gnomAD v3:
5-63965502-C-T
gnomAD v4:
5-63965502-C-T
MyVariant Identifiers:
chr5:g.63261329C>T (hg19)
chr5:g.63965502C>T (hg38)
Allelic Epigenome:
Alellic Epigenome (raw data)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.63965502C>T , CM000667.2:g.63965502C>T
GRCh38
NC_000005.9:g.63261329C>T , CM000667.1:g.63261329C>T
GRCh37
NC_000005.8:g.63297085C>T
NCBI36
NG_032816.1:g.1791G>A
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