Canonical Allele Identifier: CA117764783
Gene:

Linked Data

dbSNP Id: rs375195730

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41107333_41107334del , CM000667.2:g.41107333_41107334del GRCh38
NC_000005.9:g.41107435_41107436del , CM000667.1:g.41107435_41107436del GRCh37
NC_000005.8:g.41143192_41143193del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925944.1:n.618-5295_618-5294del
XR_925945.1:n.125-5295_125-5294del
XR_925946.1:n.576-5295_576-5294del
XR_925948.1:n.618-5295_618-5294del
XR_001742650.1:n.618-5295_618-5294del
XR_001742651.1:n.131-5295_131-5294del