Canonical Allele Identifier: CA2739274964
Gene:

Linked Data

ClinVar Variation Id: 2878787
ClinVar RCV Id: RCV003743359
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707341G>A , CM000667.2:g.112707341G>A GRCh38
NC_000005.9:g.112043038G>A , CM000667.1:g.112043038G>A GRCh37
NC_000005.8:g.112070937G>A NCBI36
NG_008481.4:g.19821G>A , LRG_130:g.19821G>A
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