Canonical Allele Identifier: CA2664269831
Gene: SSUH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733695_8733697del , CM000665.2:g.8733695_8733697del GRCh38
NC_000003.11:g.8775381_8775383del , CM000665.1:g.8775381_8775383del GRCh37
NC_000003.10:g.8750381_8750383del NCBI36
NG_008797.2:g.4886_4888del , LRG_329:g.4886_4888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8762_64+8764del ENSP00000412333.1:n.64+8762_64+8764del
ENST00000478513.1:n.335+8762_335+8764del
XR_940435.1:n.330+8762_330+8764del
XM_017006530.1:c.-283+8762_-283+8764del XP_016862019.1:n.-283+8762_-283+8764del