Canonical Allele Identifier: CA2193710013
Gene:

Linked Data

dbSNP Id: rs1894999641

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419247_87419279del , CM000677.2:g.87419247_87419279del GRCh38
NC_000015.9:g.87962478_87962510del , CM000677.1:g.87962478_87962510del GRCh37
NC_000015.8:g.85763482_85763514del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-4_368del
XR_932585.1:n.340-4_368del
XR_001751647.1:n.617-4_645del
XR_932585.2:n.627-4_655del