Canonical Allele Identifier: CA2199721327
Gene:

Linked Data

dbSNP Id: rs2059765560

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99817242dup , CM000677.2:g.99817242dup GRCh38
NC_000015.9:g.100357447dup , CM000677.1:g.100357447dup GRCh37
NC_000015.8:g.98174970dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932717.1:n.408+4156dup
XR_932718.1:n.408+4156dup
XR_932719.1:n.514+8940dup
XR_932720.1:n.409-1696dup
NR_135737.1:n.346+4156dup