Canonical Allele Identifier: CA910080444
Gene:

Linked Data

dbSNP Id: rs1441486572

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266819_72266822del , CM000665.2:g.72266819_72266822del GRCh38
NC_000003.11:g.72315970_72315973del , CM000665.1:g.72315970_72315973del GRCh37
NC_000003.10:g.72398660_72398663del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8286_835+8289del