Canonical Allele Identifier: CA850516146

Gene:

Linked Data

• dbSNP Id: rs1304166311
• MyVariant Identifiers: chr8:g.2740508C>G (hg19) ; chr8:g.2882986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2882986C>G , CM000670.2:g.2882986C>G	GRCh38
NC_000008.10:g.2740508C>G , CM000670.1:g.2740508C>G	GRCh37
NC_000008.9:g.2727915C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941367.1:n.212-42779C>G
NR_168441.1:n.1166+45222C>G
NR_168442.1:n.1331-33349C>G
NR_168443.1:n.1171+45222C>G
NR_168444.1:n.1166+45222C>G
NR_168445.1:n.1249+45139C>G