Canonical Allele Identifier: CA2723657708
Gene:

Linked Data

dbSNP Id: rs2134342394

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812695_34812698del , CM000673.2:g.34812695_34812698del GRCh38
NC_000011.9:g.34834242_34834245del , CM000673.1:g.34834242_34834245del GRCh37
NC_000011.8:g.34790818_34790821del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58088_579+58091del
XR_931188.1:n.693+58088_693+58091del
XR_931189.1:n.854+58088_854+58091del
XR_931190.1:n.639+58088_639+58091del
XR_931191.1:n.689+58088_689+58091del
XR_001748174.1:n.855+58088_855+58091del
XR_001748176.1:n.1016+58088_1016+58091del
XR_002957246.1:n.639+58088_639+58091del