Canonical Allele Identifier: CA473993915
Gene:

Linked Data

dbSNP Id: rs1856778209
MyVariant Identifiers: chr11:g.45528092del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506542del , CM000673.2:g.45506542del GRCh38
NC_000011.9:g.45528092del , CM000673.1:g.45528092del GRCh37
NC_000011.8:g.45484668del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16771del
XR_931245.3:n.566-16771del