Canonical Allele Identifier: CA1110104816
Gene:

Linked Data

dbSNP Id: rs1798578957

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907440_5907441del , CM000670.2:g.5907440_5907441del GRCh38
NC_000008.10:g.5764962_5764963del , CM000670.1:g.5764962_5764963del GRCh37
NC_000008.9:g.5752370_5752371del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7710_308-7709del
XR_941375.1:n.308-7710_308-7709del
XR_941376.1:n.406-7710_406-7709del
XR_941377.1:n.308-7710_308-7709del
XR_941378.1:n.216-7710_216-7709del
XR_001745765.1:n.308-7710_308-7709del
XR_001745766.1:n.406-7710_406-7709del
XR_001745767.1:n.216-7710_216-7709del
XR_001745768.1:n.308-7710_308-7709del
XR_941374.2:n.308-7710_308-7709del
XR_941375.2:n.308-7710_308-7709del