Canonical Allele Identifier: CA124924471
Gene:

Linked Data

ClinVar Variation Id: 506406
ClinVar RCV Id: RCV000606532
dbSNP Id: rs73216228
gnomAD v2: 5-112042929-G-A
gnomAD v3: 5-112707232-G-A
gnomAD v4: 5-112707232-G-A
MyVariant Identifiers: chr5:g.112042929G>A (hg19) chr5:g.112707232G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707232G>A , CM000667.2:g.112707232G>A GRCh38
NC_000005.9:g.112042929G>A , CM000667.1:g.112042929G>A GRCh37
NC_000005.8:g.112070828G>A NCBI36
NG_008481.4:g.19712G>A , LRG_130:g.19712G>A
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