Canonical Allele Identifier: CA1760507771
Gene:

Linked Data

dbSNP Id: rs1798579199

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907456_5907458del , CM000670.2:g.5907456_5907458del GRCh38
NC_000008.10:g.5764978_5764980del , CM000670.1:g.5764978_5764980del GRCh37
NC_000008.9:g.5752386_5752388del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7722_308-7720del
XR_941375.1:n.308-7722_308-7720del
XR_941376.1:n.406-7722_406-7720del
XR_941377.1:n.308-7722_308-7720del
XR_941378.1:n.216-7722_216-7720del
XR_001745765.1:n.308-7722_308-7720del
XR_001745766.1:n.406-7722_406-7720del
XR_001745767.1:n.216-7722_216-7720del
XR_001745768.1:n.308-7722_308-7720del
XR_941374.2:n.308-7722_308-7720del
XR_941375.2:n.308-7722_308-7720del