Canonical Allele Identifier: CA473993916

Gene:

Linked Data

• dbSNP Id: rs1204783086
• gnomAD v2: 11-45528172-CT-C
• gnomAD v3: 11-45506622-CT-C
• gnomAD v4: 11-45506622-CT-C
• MyVariant Identifiers: chr11:g.45528173del (hg19) ; chr11:g.45506623del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506625del , CM000673.2:g.45506625del	GRCh38
NC_000011.9:g.45528175del , CM000673.1:g.45528175del	GRCh37
NC_000011.8:g.45484751del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16852del
XR_931245.3:n.566-16852del