Canonical Allele Identifier: CA124924488
Gene:

Linked Data

ClinVar Variation Id: 1187671
ClinVar RCV Id: RCV001547191
dbSNP Id: rs114830579
gnomAD v2: 5-112042951-C-G
gnomAD v3: 5-112707254-C-G
gnomAD v4: 5-112707254-C-G
MyVariant Identifiers: chr5:g.112042951C>G (hg19) chr5:g.112707254C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707254C>G , CM000667.2:g.112707254C>G GRCh38
NC_000005.9:g.112042951C>G , CM000667.1:g.112042951C>G GRCh37
NC_000005.8:g.112070850C>G NCBI36
NG_008481.4:g.19734C>G , LRG_130:g.19734C>G
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