Canonical Allele Identifier: CA1573442235

Gene:

Linked Data

• ClinVar Variation Id: 1061956
• ClinVar RCV Id: RCV003652225
• dbSNP Id: rs1750554840
• gnomAD v4: 5-112707391-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707391A>G , CM000667.2:g.112707391A>G	GRCh38
NC_000005.9:g.112043088A>G , CM000667.1:g.112043088A>G	GRCh37
NC_000005.8:g.112070987A>G	NCBI36
NG_008481.4:g.19871A>G , LRG_130:g.19871A>G