Canonical Allele Identifier: CA1085192509
Gene:

Linked Data

dbSNP Id: rs1762568366

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465869_465874del , CM000668.2:g.465869_465874del GRCh38
NC_000006.11:g.465869_465874del , CM000668.1:g.465869_465874del GRCh37
NC_000006.10:g.410869_410874del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12144_2714+12149del
XR_926365.1:n.2548+12144_2548+12149del
XR_001743914.1:n.482-9339_482-9334del