ClinGen Allele Registry
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Canonical Allele Identifier:
CA101676732
Gene:
Linked Data
dbSNP Id:
rs959339310
MyVariant Identifiers:
chr4:g.100274337G>A (hg19)
chr4:g.99353180G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353180G>A , CM000666.2:g.99353180G>A
GRCh38
NC_000004.11:g.100274337G>A , CM000666.1:g.100274337G>A
GRCh37
NC_000004.10:g.100493360G>A
NCBI36
NG_011718.1:g.4581C>T
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