Canonical Allele Identifier: CA2284239380
Gene:

Linked Data

dbSNP Id: rs1968769316

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321313dup , CM000680.2:g.10321313dup GRCh38
NC_000018.9:g.10321310dup , CM000680.1:g.10321310dup GRCh37
NC_000018.8:g.10311310dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+835dup
XR_001753344.1:n.650+835dup
XR_001753345.1:n.808dup
XR_001753346.1:n.549+835dup