Canonical Allele Identifier: CA1963413228

Gene:

Linked Data

• dbSNP Id: rs1851771912

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812300_34812305del , CM000673.2:g.34812300_34812305del	GRCh38
NC_000011.9:g.34833847_34833852del , CM000673.1:g.34833847_34833852del	GRCh37
NC_000011.8:g.34790423_34790428del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57693_579+57698del
XR_931188.1:n.693+57693_693+57698del
XR_931189.1:n.854+57693_854+57698del
XR_931190.1:n.639+57693_639+57698del
XR_931191.1:n.689+57693_689+57698del
XR_001748174.1:n.855+57693_855+57698del
XR_001748176.1:n.1016+57693_1016+57698del
XR_002957246.1:n.639+57693_639+57698del