Canonical Allele Identifier: CA2664269876
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733741-CA-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733742del , CM000665.2:g.8733742del GRCh38
NC_000003.11:g.8775428del , CM000665.1:g.8775428del GRCh37
NC_000003.10:g.8750428del NCBI36
NG_008797.2:g.4933del , LRG_329:g.4933del

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8717del ENSP00000412333.1:n.64+8717del
ENST00000478513.1:n.335+8717del
XR_940435.1:n.330+8717del
XM_017006530.1:c.-283+8717del XP_016862019.1:n.-283+8717del