Canonical Allele Identifier: CA2664269891
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733750-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733754del , CM000665.2:g.8733754del GRCh38
NC_000003.11:g.8775440del , CM000665.1:g.8775440del GRCh37
NC_000003.10:g.8750440del NCBI36
NG_008797.2:g.4945del , LRG_329:g.4945del

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8708del ENSP00000412333.1:n.64+8708del
ENST00000478513.1:n.335+8708del
XR_940435.1:n.330+8708del
XM_017006530.1:c.-283+8708del XP_016862019.1:n.-283+8708del