Canonical Allele Identifier: CA229980970

Gene:

Linked Data

• dbSNP Id: rs960113661
• gnomAD v3: 11-116072464-GC-G
• gnomAD v4: 11-116072464-GC-G
• MyVariant Identifiers: chr11:g.115943183del (hg19) ; chr11:g.116072465del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116072470del , CM000673.2:g.116072470del	GRCh38
NC_000011.9:g.115943188del , CM000673.1:g.115943188del	GRCh37
NC_000011.8:g.115448398del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948055.1:n.192+549del
XR_948056.1:n.311-5260del
XR_948057.1:n.97+644del
XR_001748401.1:n.192+549del
XR_948055.2:n.192+549del
XR_948056.2:n.314-5260del
XR_948057.2:n.97+644del