Canonical Allele Identifier: CA1573442249
Gene:

Linked Data

ClinVar Variation Id: 998760
ClinVar RCV Id: RCV002241672
dbSNP Id: rs1750555732
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707400G>A , CM000667.2:g.112707400G>A GRCh38
NC_000005.9:g.112043097G>A , CM000667.1:g.112043097G>A GRCh37
NC_000005.8:g.112070996G>A NCBI36
NG_008481.4:g.19880G>A , LRG_130:g.19880G>A
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