Canonical Allele Identifier: CA802056900
Gene:

Linked Data

ClinVar Variation Id: 1014110
ClinVar RCV Id: RCV003538670
dbSNP Id: rs1173265814
MyVariant Identifiers: chr5:g.112043114G>A (hg19) chr5:g.112707417G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707417G>A , CM000667.2:g.112707417G>A GRCh38
NC_000005.9:g.112043114G>A , CM000667.1:g.112043114G>A GRCh37
NC_000005.8:g.112071013G>A NCBI36
NG_008481.4:g.19897G>A , LRG_130:g.19897G>A
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