Canonical Allele Identifier: CA676911609
Gene:

Linked Data

dbSNP Id: rs1230290600
MyVariant Identifiers: chr11:g.45528020del (hg19) chr11:g.45506470del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506471del , CM000673.2:g.45506471del GRCh38
NC_000011.9:g.45528021del , CM000673.1:g.45528021del GRCh37
NC_000011.8:g.45484597del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16699del
XR_931245.3:n.566-16699del
Search 100 bp 5'
Search 100 bp 3'