Canonical Allele Identifier: CA658655865

Gene:

Linked Data

• ClinVar Variation Id: 469899
• ClinVar RCV Id: RCV003537062
• dbSNP Id: rs1554060092
• MyVariant Identifiers: chr5:g.112043033A>G (hg19) ; chr5:g.112707336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707336A>G , CM000667.2:g.112707336A>G	GRCh38
NC_000005.9:g.112043033A>G , CM000667.1:g.112043033A>G	GRCh37
NC_000005.8:g.112070932A>G	NCBI36
NG_008481.4:g.19816A>G , LRG_130:g.19816A>G