Canonical Allele Identifier: CA915943567
Gene:

Linked Data

ClinVar Variation Id: 659284
ClinVar RCV Id: RCV003653388
dbSNP Id: rs1580995331
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707363G>A , CM000667.2:g.112707363G>A GRCh38
NC_000005.9:g.112043060G>A , CM000667.1:g.112043060G>A GRCh37
NC_000005.8:g.112070959G>A NCBI36
NG_008481.4:g.19843G>A , LRG_130:g.19843G>A
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