Canonical Allele Identifier: CA1963413214

Gene:

Linked Data

• dbSNP Id: rs1851770849
• gnomAD v3: 11-34812258-A-AT
• gnomAD v4: 11-34812258-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812263dup , CM000673.2:g.34812263dup	GRCh38
NC_000011.9:g.34833810dup , CM000673.1:g.34833810dup	GRCh37
NC_000011.8:g.34790386dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57656dup
XR_931188.1:n.693+57656dup
XR_931189.1:n.854+57656dup
XR_931190.1:n.639+57656dup
XR_931191.1:n.689+57656dup
XR_001748174.1:n.855+57656dup
XR_001748176.1:n.1016+57656dup
XR_002957246.1:n.639+57656dup