Canonical Allele Identifier: CA1573442306
Gene:

Linked Data

ClinVar Variation Id: 1010884
ClinVar RCV Id: RCV003538666
dbSNP Id: rs1213502095
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707444T>A , CM000667.2:g.112707444T>A GRCh38
NC_000005.9:g.112043141T>A , CM000667.1:g.112043141T>A GRCh37
NC_000005.8:g.112071040T>A NCBI36
NG_008481.4:g.19924T>A , LRG_130:g.19924T>A
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