Canonical Allele Identifier: CA679090676
Gene:

Linked Data

dbSNP Id: rs1194744274
gnomAD v4: 11-6318925-ATCCCTTCTCACGGAG-A
MyVariant Identifiers: chr11:g.6340156_6340170del (hg19) chr11:g.6318926_6318940del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6318928_6318942del , CM000673.2:g.6318928_6318942del GRCh38
NC_000011.9:g.6340158_6340172del , CM000673.1:g.6340158_6340172del GRCh37
NC_000011.8:g.6296734_6296748del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930997.1:n.720+708_720+722del
Search 100 bp 5'
Search 100 bp 3'