Canonical Allele Identifier: CA658655881

Gene:

Linked Data

• ClinVar Variation Id: 469863
• ClinVar RCV Id: RCV002526238
• dbSNP Id: rs1554060175
• MyVariant Identifiers: chr5:g.112043183T>C (hg19) ; chr5:g.112707486T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707486T>C , CM000667.2:g.112707486T>C	GRCh38
NC_000005.9:g.112043183T>C , CM000667.1:g.112043183T>C	GRCh37
NC_000005.8:g.112071082T>C	NCBI36
NG_008481.4:g.19966T>C , LRG_130:g.19966T>C