ClinGen Allele Registry
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Canonical Allele Identifier:
CA915943569
Gene:
Linked Data
ClinVar Variation Id:
655632
ClinVar RCV Id:
RCV003536009
dbSNP Id:
rs1580995476
gnomAD v4:
5-112707399-A-G
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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.112707399A>G , CM000667.2:g.112707399A>G
GRCh38
NC_000005.9:g.112043096A>G , CM000667.1:g.112043096A>G
GRCh37
NC_000005.8:g.112070995A>G
NCBI36
NG_008481.4:g.19879A>G , LRG_130:g.19879A>G
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