Canonical Allele Identifier: CA846801825

Gene:

Linked Data

• dbSNP Id: rs1214949234
• MyVariant Identifiers: chr8:g.124765815C>A (hg19) ; chr8:g.123753575C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123753575C>A , CM000670.2:g.123753575C>A	GRCh38
NC_000008.10:g.124765815C>A , CM000670.1:g.124765815C>A	GRCh37
NC_000008.9:g.124834996C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928607.1:n.153-11208C>A
XR_928607.3:n.324-11208C>A