Canonical Allele Identifier: CA692802675
Gene:

Linked Data

dbSNP Id: rs1354138619

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84952204dup , CM000674.2:g.84952204dup GRCh38
NC_000012.11:g.85345983dup , CM000674.1:g.85345983dup GRCh37
NC_000012.10:g.83870114dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30890dup
XR_945153.1:n.301+13740dup
XR_945154.1:n.175-36738dup
XR_945155.1:n.330+30890dup
XR_945152.2:n.316+30890dup
XR_945154.2:n.175-36738dup
XR_945155.2:n.888+30890dup