Canonical Allele Identifier: CA942311106
Gene:

Linked Data

dbSNP Id: rs1866728843

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166846_112166847del , CM000673.2:g.112166846_112166847del GRCh38
NC_000011.9:g.112037569_112037570del , CM000673.1:g.112037569_112037570del GRCh37
NC_000011.8:g.111542779_111542780del NCBI36
NG_028143.1:g.2272_2273del

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3573_320-3572del
ENST00000531744.5:c.315-3573_315-3572del ENSP00000456957.1:n.315-3573_315-3572del
ENST00000532699.1:c.315-3573_315-3572del ENSP00000456434.1:n.315-3573_315-3572del