Canonical Allele Identifier: CA1344395709
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs1707631653

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733408del , CM000665.2:g.8733408del GRCh38
NC_000003.11:g.8775094del , CM000665.1:g.8775094del GRCh37
NC_000003.10:g.8750094del NCBI36
NG_008797.2:g.4599del , LRG_329:g.4599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9051del ENSP00000412333.1:n.64+9051del
ENST00000478513.1:n.335+9051del
XR_940435.1:n.330+9051del
XM_017006530.1:c.-283+9051del XP_016862019.1:n.-283+9051del