Canonical Allele Identifier: CA675841009
Gene:

Linked Data

dbSNP Id: rs1193526788

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812312_34812318dup , CM000673.2:g.34812312_34812318dup GRCh38
NC_000011.9:g.34833859_34833865dup , CM000673.1:g.34833859_34833865dup GRCh37
NC_000011.8:g.34790435_34790441dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57705_579+57711dup
XR_931188.1:n.693+57705_693+57711dup
XR_931189.1:n.854+57705_854+57711dup
XR_931190.1:n.639+57705_639+57711dup
XR_931191.1:n.689+57705_689+57711dup
XR_001748174.1:n.855+57705_855+57711dup
XR_001748176.1:n.1016+57705_1016+57711dup
XR_002957246.1:n.639+57705_639+57711dup