Canonical Allele Identifier: CA918854987
Gene:

Linked Data

dbSNP Id: rs1565088465

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759340del , CM000673.2:g.34759340del GRCh38
NC_000011.9:g.34780887del , CM000673.1:g.34780887del GRCh37
NC_000011.8:g.34737463del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4733del
XR_931188.1:n.693+4733del
XR_931189.1:n.854+4733del
XR_931190.1:n.639+4733del
XR_931191.1:n.689+4733del
XR_001748174.1:n.855+4733del
XR_001748176.1:n.1016+4733del
XR_002957246.1:n.639+4733del