Canonical Allele Identifier: CA658655864

Gene:

Linked Data

• ClinVar Variation Id: 469901
• ClinVar RCV Id: RCV003742667
• dbSNP Id: rs1554060091
• MyVariant Identifiers: chr5:g.112043031C>T (hg19) ; chr5:g.112707334C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707334C>T , CM000667.2:g.112707334C>T	GRCh38
NC_000005.9:g.112043031C>T , CM000667.1:g.112043031C>T	GRCh37
NC_000005.8:g.112070930C>T	NCBI36
NG_008481.4:g.19814C>T , LRG_130:g.19814C>T