Canonical Allele Identifier: CA124924534
Gene:

Linked Data

ClinVar Variation Id: 1351621
ClinVar RCV Id: RCV003772446
dbSNP Id: rs370035028
MyVariant Identifiers: chr5:g.112043034G>A (hg19) chr5:g.112707337G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707337G>A , CM000667.2:g.112707337G>A GRCh38
NC_000005.9:g.112043034G>A , CM000667.1:g.112043034G>A GRCh37
NC_000005.8:g.112070933G>A NCBI36
NG_008481.4:g.19817G>A , LRG_130:g.19817G>A
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