Canonical Allele Identifier: CA972459613
Gene:

Linked Data

dbSNP Id: rs1895000322

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419286_87419310del , CM000677.2:g.87419286_87419310del GRCh38
NC_000015.9:g.87962517_87962541del , CM000677.1:g.87962517_87962541del GRCh37
NC_000015.8:g.85763521_85763545del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-39_340-15del
XR_932585.1:n.340-39_340-15del
XR_001751647.1:n.617-39_617-15del
XR_932585.2:n.627-39_627-15del