Canonical Allele Identifier: CA2664269884
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733746-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733749del , CM000665.2:g.8733749del GRCh38
NC_000003.11:g.8775435del , CM000665.1:g.8775435del GRCh37
NC_000003.10:g.8750435del NCBI36
NG_008797.2:g.4940del , LRG_329:g.4940del

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8712del ENSP00000412333.1:n.64+8712del
ENST00000478513.1:n.335+8712del
XR_940435.1:n.330+8712del
XM_017006530.1:c.-283+8712del XP_016862019.1:n.-283+8712del