Canonical Allele Identifier: CA1080214554

Gene:

Linked Data

• ClinVar Variation Id: 1063969
• ClinVar RCV Id: RCV003652232
• dbSNP Id: rs1750555884
• gnomAD v3: 5-112707402-A-G
• gnomAD v4: 5-112707402-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707402A>G , CM000667.2:g.112707402A>G	GRCh38
NC_000005.9:g.112043099A>G , CM000667.1:g.112043099A>G	GRCh37
NC_000005.8:g.112070998A>G	NCBI36
NG_008481.4:g.19882A>G , LRG_130:g.19882A>G