Canonical Allele Identifier: CA919611507
Gene:

Linked Data

dbSNP Id: rs1596084685

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419287dup , CM000677.2:g.87419287dup GRCh38
NC_000015.9:g.87962518dup , CM000677.1:g.87962518dup GRCh37
NC_000015.8:g.85763522dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-11dup
XR_932585.1:n.340-11dup
XR_001751647.1:n.617-11dup
XR_932585.2:n.627-11dup