Canonical Allele Identifier: CA2664269877
Gene: SSUH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733749_8733767dup , CM000665.2:g.8733749_8733767dup GRCh38
NC_000003.11:g.8775435_8775453dup , CM000665.1:g.8775435_8775453dup GRCh37
NC_000003.10:g.8750435_8750453dup NCBI36
NG_008797.2:g.4940_4958dup , LRG_329:g.4940_4958dup

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8697_64+8715dup ENSP00000412333.1:n.64+8697_64+8715dup
ENST00000478513.1:n.335+8697_335+8715dup
XR_940435.1:n.330+8697_330+8715dup
XM_017006530.1:c.-283+8697_-283+8715dup XP_016862019.1:n.-283+8697_-283+8715dup