Canonical Allele Identifier: CA1573442258
Gene:

Linked Data

ClinVar Variation Id: 1011102
ClinVar RCV Id: RCV003538667
dbSNP Id: rs1750556409
gnomAD v4: 5-112707406-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707406C>A , CM000667.2:g.112707406C>A GRCh38
NC_000005.9:g.112043103C>A , CM000667.1:g.112043103C>A GRCh37
NC_000005.8:g.112071002C>A NCBI36
NG_008481.4:g.19886C>A , LRG_130:g.19886C>A
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