Canonical Allele Identifier: CA2706429255

Gene:

Linked Data

• dbSNP Id: rs2110111237

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597855C>A , CM000666.2:g.89597855C>A	GRCh38
NC_000004.11:g.90519006C>A , CM000666.1:g.90519006C>A	GRCh37
NC_000004.10:g.90738029C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+9915C>A
XR_938987.1:n.433-298C>A
XR_938988.1:n.299-298C>A
XR_938990.1:n.298+9915C>A
XR_938991.1:n.298+9915C>A
XR_938992.1:n.298+9915C>A
XR_938994.1:n.643+9915C>A
XR_938995.1:n.477+9915C>A
XR_938996.1:n.298+9915C>A
XR_938997.1:n.298+9915C>A
XR_938986.2:n.323+9915C>A
XR_938987.2:n.493-298C>A