Canonical Allele Identifier: CA676911672
Gene:

Linked Data

dbSNP Id: rs1368464694
gnomAD v3: 11-45506588-AC-A
gnomAD v4: 11-45506588-AC-A
MyVariant Identifiers: chr11:g.45528139del (hg19) chr11:g.45506589del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506589del , CM000673.2:g.45506589del GRCh38
NC_000011.9:g.45528139del , CM000673.1:g.45528139del GRCh37
NC_000011.8:g.45484715del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16818del
XR_931245.3:n.566-16818del
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Search 100 bp 3'