Canonical Allele Identifier: CA1760507777
Gene:

Linked Data

dbSNP Id: rs1798579335

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907462_5907466del , CM000670.2:g.5907462_5907466del GRCh38
NC_000008.10:g.5764984_5764988del , CM000670.1:g.5764984_5764988del GRCh37
NC_000008.9:g.5752392_5752396del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7733_308-7729del
XR_941375.1:n.308-7733_308-7729del
XR_941376.1:n.406-7733_406-7729del
XR_941377.1:n.308-7733_308-7729del
XR_941378.1:n.216-7733_216-7729del
XR_001745765.1:n.308-7733_308-7729del
XR_001745766.1:n.406-7733_406-7729del
XR_001745767.1:n.216-7733_216-7729del
XR_001745768.1:n.308-7733_308-7729del
XR_941374.2:n.308-7733_308-7729del
XR_941375.2:n.308-7733_308-7729del