Canonical Allele Identifier: CA1319876327
Gene:

Linked Data

dbSNP Id: rs1701759245

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767733dup , CM000664.2:g.198767733dup GRCh38
NC_000002.11:g.199632457dup , CM000664.1:g.199632457dup GRCh37
NC_000002.10:g.199340702dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4526dup
XR_923759.1:n.72+4526dup
XR_923760.1:n.72+4526dup
XR_923759.2:n.72+4526dup
XR_923760.2:n.72+4526dup