Canonical Allele Identifier: CA2573138747
Gene:

Linked Data

ClinVar Variation Id: 1467626
ClinVar RCV Id: RCV003773025
dbSNP Id: rs1351477360
gnomAD v4: 5-112707386-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707386G>A , CM000667.2:g.112707386G>A GRCh38
NC_000005.9:g.112043083G>A , CM000667.1:g.112043083G>A GRCh37
NC_000005.8:g.112070982G>A NCBI36
NG_008481.4:g.19866G>A , LRG_130:g.19866G>A
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