Canonical Allele Identifier: CA675841064
Gene:

Linked Data

dbSNP Id: rs1471332669

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812595del , CM000673.2:g.34812595del GRCh38
NC_000011.9:g.34834142del , CM000673.1:g.34834142del GRCh37
NC_000011.8:g.34790718del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+57988del
XR_931188.1:n.693+57988del
XR_931189.1:n.854+57988del
XR_931190.1:n.639+57988del
XR_931191.1:n.689+57988del
XR_001748174.1:n.855+57988del
XR_001748176.1:n.1016+57988del
XR_002957246.1:n.639+57988del