Canonical Allele Identifier: CA220638167

Gene:

Linked Data

• dbSNP Id: rs1031175036
• gnomAD v2: 11-34780958-AAAG-A
• gnomAD v3: 11-34759411-AAAG-A
• gnomAD v4: 11-34759411-AAAG-A
• MyVariant Identifiers: chr11:g.34780959_34780961del (hg19) ; chr11:g.34759412_34759414del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34759418_34759420del , CM000673.2:g.34759418_34759420del	GRCh38
NC_000011.9:g.34780965_34780967del , CM000673.1:g.34780965_34780967del	GRCh37
NC_000011.8:g.34737541_34737543del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+4811_579+4813del
XR_931188.1:n.693+4811_693+4813del
XR_931189.1:n.854+4811_854+4813del
XR_931190.1:n.639+4811_639+4813del
XR_931191.1:n.689+4811_689+4813del
XR_001748174.1:n.855+4811_855+4813del
XR_001748176.1:n.1016+4811_1016+4813del
XR_002957246.1:n.639+4811_639+4813del