Canonical Allele Identifier: CA915943563

Gene:

Linked Data

• ClinVar Variation Id: 639358
• ClinVar RCV Id: RCV002535863
• dbSNP Id: rs1554060090

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707333G>A , CM000667.2:g.112707333G>A	GRCh38
NC_000005.9:g.112043030G>A , CM000667.1:g.112043030G>A	GRCh37
NC_000005.8:g.112070929G>A	NCBI36
NG_008481.4:g.19813G>A , LRG_130:g.19813G>A